醋酸钯

CAS: 3375-31-3 货号: P111486 分子式: C4H6O4Pd 分子量: 224.51 Beilstein号: 6086766 EC号: 222-164-4
有货
级别和纯度: ≥99.98% metals basis
别名
乙酸钯
储存条件
室温,干燥
运输条件
常规运输
★
规格
库存
价格
数量
250mg
P111486-250mg
期货 Stock Image
¥399.90
1g
P111486-1g
现货 Stock Image
¥1,132.90
5g
P111486-5g
现货 Stock Image
¥4,999.90
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为什么选择此级别

提供 ≥99.98% metals basis 纯度,适用于对基线干扰要求严格的色谱和分析工作流程。

🌡

储存与运输

室温,干燥。常规运输 。请查阅批次 COA 获取详细规格。

📋

质量文档

SDS、COA、产品数据表及规格说明书均可下载。可通过批号查询获取批次 COA。

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文献证明

在色谱分析、有机合成和交叉偶联反应领域已被 160 篇同行评审文献引用。

概述


Product class
M-O, Homogeneous Catalysts, Acetate Ligands


Reaction type
Cross Coupling Reactions with Arenes, CH-Activation, Carbonylation, Mizoroki Heck Coupling Reaction, Sonogashira-Hagihara Coupling Reaction, Suzuki-Miyaura Coupling Reaction, Oxidation


Chemical properties

Chemical formula

C12H18O12Pd3

Empirical formula

[Pd(OAc)2]3

Molecular weight

673.53

Metal

Pd

Theoretical metal content

47

Physical state

powder

Color

red brown

Applications & references

Synthesis of 2-(4-{2-[(2R)-2-Cyclopentyl-5-(5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl)-4-hydroxy-6-oxo-3,6-dihydro-2H-pyran-2-yl]-ethyl}-2-fluoro-phenyl)-2-methyl-propionitrile on multikilogram scale using a merging Heck coupling reaction. Compound is an inhibitor of the hepatitis C viral polymerase (HCVP) enzyme.


Reference: Org. Proc. Res. Dev. 2006, 10, 814. (DOI: 10.1021/op0600761)


Reductive carbonylation of aryl halides as an alternative and mild route for the introduction of aldehyde functionality, which is mostly desired for fine chemical and pharmaceutical intermediates to open up the wide range of further possible transformations.


Reference: Org. Proc. Res. Dev. 2007, 11, 39. (DOI: 10.1021/op060193w)


Synthesis of the pyrazolopyridinone-based p38 mitogen-activated protein kinase inhibitor including a Suzuki coupling reaction. p38 MAP kinases are intercellular serine/threonine kinases which certainly regulate the production and action of several pro-inflammatory mediators. They are also involved in disease states such as rheumatoid arthritis, Crohn’s diseases and psoriasis.


Reference: Org. Proc. Res. Dev. 2011, 15, 31. (DOI: 10.1021/op100205s)


Efficient hydroformylation of aryl triflates.

Reference: Synthesis 1996, 470 (DOI: 10.1055/s-1996-4246)


Deacetylation-Diazotation-Heck-Sequence: Carbon-Carbon bond formation with acetanilides as formal leaving groups


Reference: Adv. Synth. Catal. 2013, 355, 463 (DOI: 10.1002/adsc.201200929)


Deacetylation-Diazotation-Suzuki-Sequence: Carbon-Carbon bond formation with acetanilides as formal leaving groups.


Reference: Adv. Synth. Catal. 2013, 355, 463 (DOI: 10.1002/adsc.201200929)


Deacetylation-Diazotation-[2+2+1]-Cycloaddition:


Reference: Adv. Synth. Catal. 2013, 355, 463 (DOI: 10.1002/adsc.201200929)

规格

别名
乙酸钯
英文别名
Palladium (II) acetate | SR-01000389719 | EU-0040175 | BCP05504 | Palladium(II) acetate | palladium-(II) acetate | UNII-0LTG3460Y5 | Bis(acetato)palladium | Acetic Acid Palladium(II) Salt | AMY1789 | AC-677 | Diacetatopalladium | Acetic acid palladium sal
规格或纯度
≥99.98% metals basis
英文名称
Palladium acetate
储存条件
室温,干燥
运输条件
常规运输
法律信息
Product of Umicore
纯度
≥99.98% metals basis
名称和识别符
PubChem SID
EC号
222-164-4
分子类型
小分子
IUPAC Name
palladium(2+);diacetate
INCHI
1S/2C2H4O2.Pd/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
InChi Key
YJVFFLUZDVXJQI-UHFFFAOYSA-L
Smiles
CC(=O)[O-].CC(=O)[O-].[Pd+2]
Isomeric SMILES
CC(=O)[O-].CC(=O)[O-].[Pd+2]
UN Number
Packing Group
III
分子量
224.51
Beilstein号
6086766
Reaxy-Rn
3602276
Reaxys-RN link address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3602276&ln=

技术文档

📋 安全数据表 (SDS)

全面的危险、操作、储存及法规合规文件。

下载 SDS →

✅ 分析证书 (COA)

批次质量数据。输入批号以获取对应 COA。

查询 COA →

📊 产品数据表

产品规格和应用的快速参考摘要。

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🔬 规格说明书

该级别的完整质量属性和验收标准。

查看规格说明 →

高级数据

系统学分类

分类树(Taxonomy Tree)

界(kingdom) 有机化合物
超类(Superclass) 有机酸及其衍生物
类(Class) 羧酸及其衍生物
亚类(Subclass) 羧酸
中间层级节点(Intermediate Tree Nodes) 暂无
直接上位类(Direct Parent) 羧酸
其他上位类(Alternative Parents) 一元羧酸及其衍生物  有机盐  有机氧化物  碳氢化合物衍生物  羰基化合物  
分子骨架(Molecular Framework) 暂无
取代基(Substituents) 脂肪族非环化合物 - 羰基 - 羧酰胺基 - 烃衍生物 - 单羧酸或其衍生物 - 有机氧化物 - 有机氧化合物 - 有机盐 - 有机氧化合物
描述(Description) 该化合物属于有机化合物中的羧酸类。这类化合物含有羧基,其化学式为-C(=O)OH。
外部描述符(External Descriptors) 暂无
三维结构
交互式化学结构模型





化学和物理性质
密度
0.984
熔点
216.3-223.7°C
分子量
224.510 g/mol
XLogP3
氢键供体数Hydrogen Bond Donor Count
0
氢键受体数Hydrogen Bond Acceptor Count
4
可旋转键计数Rotatable Bond Count
0
精确质量Exact Mass
223.93 Da
单同位素质量Monoisotopic Mass
223.93 Da
拓扑极表面积Topological Polar Surface Area
80.300 Ų
重原子数Heavy Atom Count
9
形式电荷Formal Charge
0
复杂度Complexity
25.500
同位素原子数Isotope Atom Count
0
定义的原子立体中心计数Defined Atom Stereocenter Count
0
未定义的原子立体中心计数Undefined Atom Stereocenter Count
0
定义的键立体中心计数Defined Bond Stereocenter Count
0
未定义的键立体中心计数Undefined Bond Stereocenter Count
0
所有立体化学键的总数The total count of all stereochemical bonds
0
共价键合单元计数Covalently-Bonded Unit Count
3
安全和危险性(GHS)
象形图
GHS05,   GHS07,   GHS09
信号词
危险
危险声明

H302: 吞食有害

H317: 可能引起皮肤过敏反应

H318: 造成严重的眼睛损伤

H400: 对水生生物有剧毒

H410: 对水生生物有剧毒并具有长期持续影响

预防措施声明

P261: 避免吸入灰尘/烟雾/气体/雾/蒸汽/喷雾

P264: 处理后要彻底洗手。

P270: 使用本产品时,请勿进食、饮水或吸烟。

P272: 被污染的工作服不允许离开工作场所

P273: 避免释放到环境中。

P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。

P321: 特殊处理(请参阅此标签上的...)。

P330: 漱口

P391: 收集溢出物

P302+P352: 如皮肤沾染:用水充分清洗。

P333+P313: 如发生皮肤刺激或皮疹:求医/就诊。

P362+P364: 脱掉沾污的衣服,清洗后方可重新使用。

P501: 将内容物/容器处理到。。。

P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。

P301+P317: 如果被吞咽:请寻求医疗帮助。

P305+P354+P338: 如果进入眼睛:立即用水冲洗几分钟。取下隐形眼镜(如果有的话),并且操作简单。继续冲洗。

P317: 寻求紧急医疗救助。

WGK Germany
3
RTECS
AJ1900000
Class
9
Merck Index
6991
个人防护装备
dust mask type N95 (US),Eyeshields,Gloves
质检证书(CoA,COO,BSE/TSE 和分析图谱)
C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:

通过匹配包装上的批号来查找并下载产品的 COA,每批产品都进行了严格的验证,您可放心使用!

找到15个结果

批号(Lot Number) 证书类型 货号
K2208405 分析证书 P111486
K2208465 分析证书 P111486
B2628585 分析证书 P111486
B2628586 分析证书 P111486
B2628607 分析证书 P111486
B2628608 分析证书 P111486
B2628609 分析证书 P111486
B2628610 分析证书 P111486
B2628611 分析证书 P111486
A2627073 分析证书 P111486
L2102656 分析证书 P111486
F2512033 分析证书 P111486
I2522050 分析证书 P111486
F2215226 分析证书 P111486
F2215238 分析证书 P111486
技术文档和文章
白介素—免疫应答的通讯部队
Interleukins - the communications arm of the immune response
丙烯腈
Acrylonitrile
1-氟-2,4,6-三甲基吡啶三氟甲烷磺酸盐
N-Fluoro-2,4,6-trimethylpyridinium triflate
White催化剂
White Catalyst
聚甲基氢硅氧烷(PMHS)
钯催化反应一站式手册:催化循环、失活排查、配体/预催化剂选型与阿拉丁清单
One-Stop Handbook for Palladium-Catalyzed Reactions: Catalytic Cycles, Deactivation Troubleshooting, Ligand/Precatalyst Selection, and an Aladdin Reference List
从哌啶到吡啶:2013–2023 FDA 小分子新药里“最常见含氮杂环”更替与选型导航(表1–4)
From Piperidine to Pyridine: The “Most Common N-Heterocycle” Shift in FDA Small-Molecule New Drugs (2013–2023) and a Selection Guide (Tables 1–4)
合成锌试剂(Organozinc Reagents)实用指南:结构特性、关键反应与实用选型导航(含阿拉丁产品表)
A Practical Guide to Organozinc Reagents for Synthesis (Organozinc Reagents): Structural Features, Key Reactions, and a Practical Selection Navigation (Including Aladdin Product Tables)
贵金属盐/前驱体选型指南:从真实物种到可复现起点(含产品导航与表1–表3)
Selection Guide to Precious-Metal Salts & Precursors: From Speciation to a Reproducible Starting Point (with Product Navigator and Tables 1–3)
过渡金属盐/前驱体选型导览:同金属不同盐的起点差异与复现要点(含选型导航及产品表1–表5)
Transition-Metal Salts/Precursor Selection Guide: How “Different Salts of the Same Metal” Start from Different Chemical Realities—and How to Reproduce Results (including a Selection Navigator and Product Tables 1–5)
把“芳基氯 + 低Pd + 放大复现”做稳:Pd–NHC(钯-N-杂环卡宾)交叉偶联的启动与耐久逻辑(含选型导航与产品表)
Make “Aryl Chlorides + Low Pd Loading + Scale-Up Reproducibility” Reliable: The Initiation and Durability Logic of Pd–NHC (Palladium–N-Heterocyclic Carbene) Cross-Coupling (with Selection Navigation and Product Tables)
把反应做稳的硼源选择:硼酸、硼酸酯、BF₃K 与 MIDA 如何提升 Suzuki–Miyaura 的起速与放大复现 (含产品表1–5)
Choosing Boron Sources to Make Reactions Robust: How Boronic Acids, Boronate Esters, BF₃K Salts, and MIDA Improve Suzuki–Miyaura Start-Up and Scale-Up Reproducibility (with Product Tables 1–5)
Suzuki–Miyaura 反应怎么做稳:定位瓶颈,锁定可复现窗口(含选型导航及产品表1–表5)
How to Make the Suzuki–Miyaura Reaction Robust: Pinpoint the Bottleneck and Lock in a Reproducible Operating Window (with Selection Navigation and Product Tables 1–5)
腈基如何构建:直接引入、前体脱水、氧化/脱氢与无氰工艺的路线判断
How to Construct Nitriles: Route Selection Across Direct Introduction, Precursor Dehydration, Oxidation/Dehydrogenation, and Cyanide-Free Processes
C-C键构建的实验选型逻辑:按成键任务理解片段偶联、羰基延链、烯基化及后期成键路径
Experimental Selection Logic for C-C Bond Construction: Understanding Fragment Coupling, Carbonyl Chain Extension, Olefination, and Late-Stage Bond-Forming Pathways by Bond-Forming Task
小分子合成中的反应选择:从转化类型判断到实验路径筛选
Reaction Selection in Small-Molecule Synthesis: From Transformation-Type Assessment to Experimental Route Screening
过渡金属催化 C–H 官能团化的实验选型逻辑:何时值得做,如何判断位点与条件
Experimental Selection Logic for Transition-Metal-Catalyzed C–H Functionalization: When It Is Worth Pursuing and How to Assess Site Selectivity and Conditions
交叉偶联反应的实验判断方法:目标键型、底物组合与催化体系选择
Experimental Decision-Making for Cross-Coupling Reactions: Target Bond Type, Substrate Combination, and Catalytic System Selection
PMHS, Polymethylhydrosiloxane
羟烷基取代芳基/烯基硼酸酯脱氧氟化:经 BF3K 中间体实现 C–F 键构建与 C–B 键保留
Deoxyfluorination of Hydroxyalkyl-Substituted Aryl/Alkenyl Boronates: C–F Bond Construction and C–B Bond Retention via a BF3K Intermediate
CTSOBt 苯并三氮唑-磺酸酯缩合试剂:羧酸活化与合成应用价值
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
吲唑骨架的药物化学设计:互变异构、分子识别、取代位点设计与合成策略
Medicinal Chemistry Design of the Indazole Scaffold: Tautomerism, Molecular Recognition, Substitution-Site Design, and Synthetic Strategies
哌啶C–H官能团化的选择性从何而来?——氮原子效应、椅式构象与四类关键中间体
Where Does the Selectivity in Piperidine C–H Functionalization Come From? — Nitrogen Effects, Chair Conformations, and Four Classes of Key Intermediates
固态甲醇钠和乙醇钠的空气分解——对交叉偶联反应优化与重现性的影响
Air Decomposition of Solid Sodium Methoxide and Sodium Ethoxide—Effects on Cross-Coupling Reaction Optimization and Reproducibility
此产品的引用文献
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