为了获得访问"阿拉丁铁蛋"实时聊天框的流畅支持体验,建议您使用Chrome浏览器或选择360浏览器极速模式(如何切换极速模式?),感谢您选择我们!

1-(叔丁氧羰基)哌嗪

规格或纯度: 98%
有货

库存信息

关闭

库存信息

关闭

库存信息

关闭

库存信息

关闭

库存信息

关闭
货号 (SKU) 包装规格 是否现货 价格 数量
B106917-1g
1g 现货 Stock Image
B106917-5g
5g 现货 Stock Image
B106917-25g
25g 现货 Stock Image
B106917-100g
100g 现货 Stock Image
B106917-500g
500g 现货 Stock Image
查看相关系列
哌嗪类 杂环砌块

基本描述

别名 1-Boc-哌嗪 | 哌嗪-1-甲酸叔丁酯 | 哌嗪-1-甲酸叔丁酯
英文别名 1 -t-butoxycarbonyl piperazine | 1-[1,1-dimethylethoxycarbonyl]piperazine | 1-boc piperazine | n-tert-butyloxycarbonylpiperazine | N-tert-butyloxycarbonyl-piperazine | tert-butyl-1-piperazinecarboxylate | tertbutyl-1-piperazinecarboxylate | 1-(t-butoxycar
规格或纯度 98%
英文名称 1-Boc-piperazine
应用 · (m·-苯氧基)苯基取代哌嗪衍生物系列的制备 · 通过活性阳离子开环聚合合成α,β-聚(2-噁唑啉)脂聚合物期间的终止步骤。 · 单取代哌嗪的制备,例如吲唑脱氧核糖核酸回旋酶抑制剂的合成
储存温度 2-8°C储存,充氩
运输条件 冰袋运输
产品介绍

1-Boc-哌嗪与各种芳基卤化物发生 Buchwald-Hartwig 胺化反应,形成相应的的胺衍生物。它可用于合成许多生物活性分子的单取代哌嗪中间体和含有哌嗪的原料药,如曲唑酮。

1-Boc-piperazine is an N-Boc protected piperazine. Crosscoupling of 1-Boc-piperazine with aryl iodides using CuBr/1,1′-bi-2-naphthol (catalyst) and K3PO4 (base) has been reported.1-Boc-piperazine undergoes Buchwald-Hartwig coupling reactions with aryl halides.1-Boc-piperazine can be prepared in 80% yield via solvent-free N-Boc protection catalyzed by iodine
1-Boc-piperazine was used in Buchwald-Hartwig coupling reaction

名称和标识符

EC号 MFCD00075265
IUPAC Name tert-butyl piperazine-1-carboxylate
INCHI InChI=1S/C9H18N2O2/c1-9(2,3)13-8(12)11-6-4-10-5-7-11/h10H,4-7H2,1-3H3
InChi Key CWXPZXBSDSIRCS-UHFFFAOYSA-N
Canonical SMILES CC(C)(C)OC(=O)N1CCNCC1
Isomeric SMILES CC(C)(C)OC(=O)N1CCNCC1
WGK Germany 3
关联CAS 143238-38-4
PubChem CID 143452
分子量 186.25
Beilstein号 879985
Reaxy-Rn 879985

化学和物理性质

溶解性 Soluble in ethyl acetate, methanol and water.
密度 1.03
敏感性 对空气敏感;易吸湿; 对热敏感
闪点(℉) 235.4 °F
闪点(℃) 113 °C
熔点 43-47°C

安全和危险性(GHS)

象形图
ghs07

Harmful

信号词 Danger
危险声明 H315: Causes skin irritation
H319: Causes serious eye irritation
预防措施声明 P261,P305+P351+P338,P280,P302+P352,P321,P405,P501,P264,P260,P271,P301+P330+P331,P304+P340,P363,P403+P233,P362+P364,P264+P265,P305+P354+P338,P337+P317,P332+P317,P302+P361+P354,P316,P319
WGK Germany 3
Reaxy-Rn 879985
个人防护装备 dust mask type N95 (US),Eyeshields,Gloves

质检证书(COA)

质检报告(COA)

输入批号以搜索COA:

相关文档

质检报告COA

请输入批号:


产品问答

产品问答

登录提交问题 Hover me 请先登录再提交问题
您提交该产品问题后,我们会在1-2个工作日内给您答复,您可以登录"我的账号",然后点击"我的产品问答"查看答案

参考文献

1. Florencio Zaragoza,Henrik Stephensen,Sanne M Knudsen,Lone Pridal,Birgitte S Wulff,Karin Rimvall.  (2004-05-14)  1-alkyl-4-acylpiperazines as a new class of imidazole-free histamine H(3) receptor antagonists..  Journal of medicinal chemistry,  47  ((11)):  (2833-2838).  [PMID:15139761]
2. Ravi Varala,Sreelatha Nuvula,Srinivas R Adapa.  (2006-10-10)  Molecular iodine-catalyzed facile procedure for N-Boc protection of amines..  The Journal of organic chemistry,  71  ((21)):  (8283-8286).  [PMID:17025327]
3. Dengfeng Dou,Guijia He,Sivakoteswara Rao Mandadapu,Sridhar Aravapalli,Yunjeong Kim,Kyeong-Ok Chang,William C Groutas.  (2011-11-29)  Inhibition of noroviruses by piperazine derivatives..  Bioorganic & medicinal chemistry letters,  22  ((1)):  (377-379).  [PMID:22119464]
4. Akihiko Tanitame,Yoshihiro Oyamada,Keiko Ofuji,Yoko Kyoya,Kenji Suzuki,Hideaki Ito,Motoji Kawasaki,Kazuo Nagai,Masaaki Wachi,Jun-ichi Yamagishi.  (2004-05-06)  Design, synthesis and structure-activity relationship studies of novel indazole analogues as DNA gyrase inhibitors with Gram-positive antibacterial activity..  Bioorganic & medicinal chemistry letters,  14  ((11)):  (2857-2862).  [PMID:15125947]
5. Nisar Ullah.  (2013-03-16)  Synthesis and dual D2 and 5-HT1A receptor binding affinities of 5-piperidinyl and 5-piperazinyl-1H-benzo[d]imidazol-2(3H)-ones..  Journal of enzyme inhibition and medicinal chemistry,  29  ((2)):  (281-291).  [PMID:23488743]