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O-叔丁基羟胺 盐酸盐_分子结构_CAS_39684-28-1)
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O-叔丁基羟胺 盐酸盐

产品号 B5765 公司名称 Sigma Aldrich
CAS号 39684-28-1 公司网站 http://www.sigmaaldrich.com
分子式 C4H12ClNO 电 话 1-800-521-8956
分子量 125.59718 传 真
纯 度 ≥99% 电子邮件
保 存 Chembase数据库ID: 81897

产品价格信息

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产品别名

标题
O-tert-Butylhydroxylamine hydrochloride
IUPAC标准名
O-tert-butylhydroxylamine hydrochloride
IUPAC传统名
O-tert-butylhydroxylamine hydrochloride
别名
tert-Butoxyamine hydrochloride
O-(1,1-Dimethylethyl)hydroxylamine hydrochloride
2-Aminooxy-2-methylpropane hydrochloride

产品登记号

Beilstein号 3668106
MDL号 MFCD00043272
PubChem SID 24891858
CAS号 39684-28-1
EC号 254-590-1

产品性质

线性分子式 (CH3)3CONH2 · HCl
纯度 ≥99%
GHS危险品标识 GHS02
GHS警示词 Warning
GHS危险声明 H228
欧盟危险性物质标志 易燃性(Flammable) 易燃性(Flammable) (F)
MSDS下载 下载链接
个人保护装置 Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS警示性声明 P210
RID/ADR UN 1325 4.1/PG 3
危险公开号 11
联合国危险货物等级 4.1
联合国危险货物编号 1325
联合国危险货物包装类别(PG) 3
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
5 g in glass bottle
Application
Reactant involved in synthesis of biologically active molecules including:
• CGS 25966 derivatives for use as MMP inhibitors1
• Imidazolidinedione derivatives for use as antimalarial treatments2
• Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists3
• Rab proteins for isoprenylation and geranylgeranylation inhibition4Reactant involved in:
• Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents5
• Double allylic alkylation of indole-2-hydroxamates6
• SN2 substitution reactions at amide nitrogens7
• Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines8
详细说明 (简体中文)
包装
5 g in glass bottle
Application
Reactant involved in synthesis of biologically active molecules including:
• CGS 25966 derivatives for use as MMP inhibitors1
• Imidazolidinedione derivatives for use as antimalarial treatments2
• Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists3
• Rab proteins for isoprenylation and geranylgeranylation inhibition4Reactant involved in:
• Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents5
• Double allylic alkylation of indole-2-hydroxamates6
• SN2 substitution reactions at amide nitrogens7
• Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines8

参考文献