概述规格名称和识别符技术文档高级数据系统学分类三维结构作用机制质检证书（CoA,COO,BSE/TSE 和分析图谱) 化学和物理性质安全和危险性（GHS）此产品的引用文献技术文档和文章引用文献溶液计算器

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为什么选择此级别

提供 ≥96% 纯度，适用于对基线干扰要求严格的色谱和分析工作流程。

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储存与运输

-20°C储存,充氩。超低温运输,DG运输。请查阅批次 COA 获取详细规格。

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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 71 篇同行评审文献引用。

概述

有刺激性气味，溶于酮、醚等有机溶剂中，在水和乙醇中分解。用于有机合成的中间体。

规格

别名

苯甲氧羰酰氯 | 苄氧羰基氯 | 苯甲氧基甲酰氯

英文别名

规格或纯度

≥96%, contains 0.1% sodium carbonate as stabilizer

英文名称

Benzyl chloroformate(Cbz-Cl)

储存条件

-20°C储存,充氩

运输条件

超低温运输,DG运输

纯度

≥96%

名称和识别符

PubChem SID

528772738

EC号

207-925-0

分子类型

小分子

IUPAC Name

benzyl carbonochloridate

INCHI

1S/C8H7ClO2/c9-8(10)11-6-7-4-2-1-3-5-7/h1-5H,6H2

InChi Key

HSDAJNMJOMSNEV-UHFFFAOYSA-N

Smiles

C1=CC=C(C=C1)COC(=O)Cl

Isomeric SMILES

C1=CC=C(C=C1)COC(=O)Cl

UN Number

1739

Packing Group

分子量

170.59

Beilstein号

509751

Reaxy-Rn

509751

Reaxys-RN link address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=509751&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。

查看数据表 →

🔬 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) 苯类化合物
  - 类（Class) 苯及其取代衍生物
    - 亚类（Subclass）苄氧羰基

界（kingdom)	有机化合物
超类（Superclass)	苯类化合物
类（Class)	苯及其取代衍生物
亚类（Subclass）	苄氧羰基
中间层级节点（Intermediate Tree Nodes）	暂无
直接上位类(Direct Parent)	苄氧羰基
其他上位类（Alternative Parents）	有机碳酸及其衍生物有机氯化物有机氧化物碳氢化合物衍生物羰基化合物
分子骨架（Molecular Framework)	芳香族同单环化合物
取代基（Substituents）	芳香族同单环化合物 - 苄氧羰基 - 碳酸衍生物 - 羰基 - 烃衍生物 - 有机氧化物 - 有机氧化合物 - 有机氯化物 - 有机卤化物 - 有机氧化合物
描述（Description）	该化合物属于苯甲氧羰基类有机化合物。这类化合物含有被苯甲氧基取代的羰基。
外部描述符（External Descriptors）	暂无

三维结构

交互式化学结构模型

球棍
棍棒
线框模型
空间填充
显示氢气
动画

作用机制

作用机制	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	参考文献

化学和物理性质

溶解性

Miscible with ether, acetone and benzene

密度

1.195

敏感性

对热和湿度敏感

折光率

1.516-1.518

闪点(℉)

92℃

闪点(℃)

92℃

沸点

130℃/20mmHg

熔点

-20°C

分子量

170.590 g/mol

XLogP3

3.000

氢键供体数Hydrogen Bond Donor Count

氢键受体数Hydrogen Bond Acceptor Count

可旋转键计数Rotatable Bond Count

精确质量Exact Mass

170.013 Da

单同位素质量Monoisotopic Mass

170.013 Da

拓扑极表面积Topological Polar Surface Area

26.300 Å²

重原子数Heavy Atom Count

形式电荷Formal Charge

复杂度Complexity

130.000

同位素原子数Isotope Atom Count

定义的原子立体中心计数Defined Atom Stereocenter Count

未定义的原子立体中心计数Undefined Atom Stereocenter Count

定义的键立体中心计数Defined Bond Stereocenter Count

未定义的键立体中心计数Undefined Bond Stereocenter Count

所有立体化学键的总数The total count of all stereochemical bonds

共价键合单元计数Covalently-Bonded Unit Count

安全和危险性（GHS）

一般危化品

象形图

GHS05, GHS09

信号词

危险

危险声明

H314: 造成严重的皮肤灼伤和眼睛损伤

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

P260: 不要吸入灰尘/烟雾/气体/雾/蒸汽/喷雾。

P264: 处理后要彻底洗手。

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...）。

P363: 再次使用之前，请清洗受污染的衣物。

P391: 收集溢出物

P301+P330+P331: 如误吞咽：漱口。不要诱导呕吐。

P304+P340: 如误吸入：将人转移到空气新鲜处，保持呼吸舒适体位。

P405: 密闭存放

P501: 将内容物/容器处理到。。。

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。

P302+P361+P354: 如果接触皮肤：立即脱掉所有被污染的衣服。立即用水冲洗几分钟。

P316: 立即寻求紧急医疗救助。

WGK Germany

RTECS

LQ5860000

Class

Merck Index

1801

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28个结果

批号(Lot Number)	证书类型	货号
H2625232	分析证书	B105737
H2625231	分析证书	B105737
H2625230	分析证书	B105737
H2625229	分析证书	B105737
L2313037	分析证书	B105737
C2513188	分析证书	B105737
K2301050	分析证书	B105737
J2323098	分析证书	B105737
E2211026	分析证书	B105737
D2620071	分析证书	B105737
A2614213	分析证书	B105737
A2614214	分析证书	B105737
A2614215	分析证书	B105737
K2528055	分析证书	B105737
A2214319	分析证书	B105737
G2524044	分析证书	B105737
C2427123	分析证书	B105737
C2427124	分析证书	B105737
G2528063	分析证书	B105737
G2528064	分析证书	B105737
G2528065	分析证书	B105737
C2427122	分析证书	B105737
C2427117	分析证书	B105737
A2214318	分析证书	B105737
A2214332	分析证书	B105737
G2415319	分析证书	B105737
E2211020	分析证书	B105737
E2211019	分析证书	B105737

显示更多⌵

技术文档和文章

认识 Cbz（苄氧羰基）：经典氨基保护基的选用思路与应用价值

目录：技术文章

探索主题:

苄氧羰基含胺有机合成氨基保护基

Understanding Cbz (Benzyloxycarbonyl): Selection Logic and Practical Value of a Classical Amino Protecting Group

目录：技术文章

探索主题:

benzyloxycarbonyl Organic synthesis containing amines Amino protecting group

重新认识 N-酰基型氨基保护基：Ac、Bz 与 Tfa 的脱保护差异、路线分工与实验选用思路

目录：技术文章

探索主题:

保护基乙酰基苯甲酰基三氟乙酰基 N-酰基型保护

Reconsidering N-Acyl Amino Protecting Groups: Deprotection Differences, Strategic Roles, and Experimental Selection of Ac, Bz, and Tfa

目录：技术文章

探索主题:

protecting group acetyl benzoyl trifluoroacetyl N-acyl protection

多肽合成路线的判断逻辑：从 SPPS、LPPS 到重组表达的适用情形与判断依据

目录：技术文章

探索主题:

多肽合成液相多肽合成多肽化学制备

Decision Logic for Peptide Synthesis Routes: Applicability and Criteria for Choosing among SPPS, LPPS, and Recombinant Expression

目录：技术文章

探索主题:

Peptide synthesis Liquid-phase peptide synthesis

Teoc 氨基保护基的选用逻辑：从氟离子触发脱保护到正交保护设计

目录：技术文章

探索主题:

保护基官能团

Selection Logic for the Teoc Amino Protecting Group: From Fluoride-Triggered Deprotection to Orthogonal Protecting-Group Design

目录：技术文章

探索主题:

protecting group Functional Group

Boc₂O 的选用不能只看保护引入：从底物亲核性、介质效应到脱保护路径的实验判断

目录：技术文章

探索主题:

氨基甲酸酯 Boc₂O Boc 保护

Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways

目录：技术文章

探索主题:

Boc₂O carbamate Boc protection

三光气在有机合成中的实验判断：按反应任务理解其选用逻辑

目录：技术文章

探索主题:

有机合成三光气

Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks

目录：技术文章

探索主题:

Organic synthesis Triphosgene

多肽合成异常杂质如何排查？从氨基相关副反应看工艺问题定位

目录：技术文章

探索主题:

多肽合成固相多肽合成异常杂质

How to Troubleshoot Abnormal Impurities in Peptide Synthesis? Locating Process Issues Through Amino-Related Side Reactions

目录：技术文章

探索主题:

Peptide synthesis Solid phase peptide synthesis Abnormal impurities

什么是多胺？结构特点、分类与代表物、应用及合成策略

目录：技术文章

探索主题:

有机化学药物化学多胺含氮有机化合物多个胺型氮原子

What Are Polyamines? Structural Features, Classification and Representative Compounds, Applications, and Synthetic Strategies

目录：技术文章

探索主题:

Organic chemistry Medicinal Chemistry Polyamine Multiple amine nitrogen atoms Nitrogen-containing organic compounds

AITF 介导羧酸活化用于酰胺、肽和酯合成：活化机制与适用场景

目录：技术文章

探索主题:

酰胺键肽键酯键 AITF

AITF-Mediated Carboxylic Acid Activation for the Synthesis of Amides, Peptides, and Esters: Activation Mechanism and Applicable Scenarios

目录：技术文章

探索主题:

Peptides AITF Amides Esters

桥头位 α-氟胺的稳定化设计及其药物化学砌块价值

目录：技术文章

探索主题:

脂肪族胺氟原子

Stabilization Design of Bridgehead α-Fluoroamines and Their Value as Medicinal Chemistry Building Blocks

目录：技术文章

探索主题:

Aliphatic amine Fluorine atom

CTSOBt 苯并三氮唑-磺酸酯缩合试剂：羧酸活化与合成应用价值

目录：技术文章

探索主题:

多肽合成羧酸活化缩合试剂

CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value

目录：技术文章

探索主题:

Peptide synthesis coupling reagent coupling reagents

氮杂三环烷烃的张力释放：三维氮杂桥环的桥位模块化官能团化与立体控制

目录：技术文章

探索主题:

ABCAs 氮杂双环[x.1.1]烷烃

Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds

目录：技术文章

探索主题:

ABCAs azabicyclo[x.1.1]alkanes

O-乙烯基羟胺构建7-氮杂吲哚：N-氧化物活化与[3,3]-σ迁移重排

目录：技术文章

探索主题:

7-氮杂吲哚

Construction of 7-Azaindoles Using O-Vinylhydroxylamines: N-Oxide Activation and [3,3]-Sigmatropic Rearrangement

目录：技术文章

探索主题:

7-Azaindoles

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

目录：技术文章

探索主题:

哌啶氮原子效应

Where Does the Selectivity in Piperidine C–H Functionalization Come From? — Nitrogen Effects, Chair Conformations, and Four Classes of Key Intermediates

目录：技术文章

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Piperidine Nitrogen Effects

含氟3,3-二取代氧杂环丁烷砌块的设计逻辑：结构构建及胺碱性、亲脂性与代谢稳定性调节

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分子砌块含氟氧杂环丁烷 3,3-二取代氧杂环丁烷胺碱性 pKₐ logP logD 微粒体稳定性匹配分子对

Design Logic of Fluorinated 3,3-Disubstituted Oxetane Building Blocks: Structural Construction and Modulation of Amine Basicity, Lipophilicity, and Metabolic Stability

目录：技术文章

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pKₐ logP logD fluorinated oxetane 3,3-disubstituted oxetane molecular building block amine basicity microsomal stability matched molecular pair

先构建三元环，还是先形成碳—氮键？——环丙胺合成的逆合成策略、路线选择与立体控制

目录：技术文章

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对映选择性环丙胺氨基环丙烷 N-环丙基胺逆合成分析碳—氮键形成环丙烷化环张力区域选择性非对映选择性 Kulinkovich反应

Build the Three-Membered Ring First, or Form the Carbon–Nitrogen Bond First?—Retrosynthetic Strategies, Route Selection, and Stereochemical Control in Cyclopropylamine Synthesis

目录：技术文章

探索主题:

Enantioselectivity cyclopropylamines aminocyclopropanes N-cyclopropylamines retrosynthetic analysis carbon–nitrogen bond formation cyclopropanation ring strain regioselectivity diastereoselectivity Kulinkovich reaction

氮丙啶在药物合成中的构建与转化：环张力、N-取代调控、选择性开环与骨架扩展

目录：技术文章

探索主题:

氮杂环丁烷药物合成环张力区域选择性氮丙啶 N-取代效应立体专一性对映汇聚交叉亲电偶联 β-取代胺

Construction and Transformation of Aziridines in Drug Synthesis: Ring Strain, N-Substituent Control, Selective Ring Opening, and Scaffold Expansion

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LY3509754关键α-溴代酮的构建：β-氧代酯策略与酶促酯水解后的伴随脱羧

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Construction of the Key α-Bromoketone Intermediate for LY3509754: A β-Keto Ester Strategy and Concomitant Decarboxylation Following Enzymatic Ester Hydrolysis

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Small molecule inhibitors

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12. Yixuan Xia, Zhigang Xiao, Yinhui Yi, Tingting Liu, Conglin Zhang, Gangbing Zhu. (2022) Nitrogen-doped hollow bowl-like carbon as highly effective sensing material for electroanalysis. MICROCHEMICAL JOURNAL, [10.1016/j.microc.2022.108094]
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