产品名称

英文名称：O-tert-ButylhydroxylamineHydrochloride

同义词

39684-28-1、O-tert-Butylhydroxylamine hydrochloride、O-(tert-Butyl)hydroxylamine hydrochloride、O-tert-butylhydroxylamine;hydrochloride、O-t-Butylhydroxylamine hydrochloride、tert-butoxyamine hydrochloride、Hydroxylamine, O-(1,1-dimethylethyl)-, hydrochloride、M、叔丁氧胺盐酸盐、邻叔丁基羟胺盐酸盐

产品性质

CAS编号：39684-28-1

分子式：(CH3)3CONH2 · HCl

分子量：125.6

Beilstein号：3668106

EC号：254-590-1

MDL号：MFCD00043272

PubChem编号：2777906

别名：叔丁氧胺盐酸盐|邻叔丁基羟胺盐酸盐

英文别名：39684-28-1|O-tert-Butylhydroxylamine hydrochloride|O-(tert-Butyl)hydroxylamine hydrochloride|O-tert-butylhydroxylamine;hydrochloride|O-t-Butylhydroxylamine hydrochloride|tert-butoxyamine hydrochloride|Hydroxylamine, O-(1,1-dimethylethyl)-, hydrochloride|M

规格或纯度：≥98%

英文名称：O-tert-ButylhydroxylamineHydrochloride

应用：Reactant involved in synthesis of biologically active molecules including<BR/>· CGS 25966 derivatives for use as MMP inhibitors· Imidazolidinedione derivatives for use as antimalarial treatments<BR>· Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists<BR>· Rab proteins for isoprenylation and geranylgeranylation inhibition<BR/>Reactant involved in<BR/>· Synthesis of <I>N</I>-(arylethyl)-<I>O</I>-<I>tert</I>-butylhydroxamates for use as Weinreb amide equivalents· Double allylic alkylation of indole-2-hydroxamates· SN2 substitution reactions at amide nitrogens· Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines<BR>

储存温度：充氩

运输条件：常规运输

产品介绍：Reactant involved in synthesis of biologically active molecules including· CGS 25966 derivatives for use as MMP inhibitors· Imidazolidinedione derivatives for use as antimalarial treatments· Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists· Rab proteins for isoprenylation and geranylgeranylation inhibitionReactant involved in· Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents· Double allylic alkylation of indole-2-hydroxamates· SN2 substitution reactions at amide nitrogens· Photocycloaddition to C=N bonds for synthesis of 1,3-diazepinesReactant involved in synthesis of biologically active molecules including· CGS 25966 derivatives for use as MMP inhibitors· Imidazolidinedione derivatives for use as antimalarial treatments· Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists· Rab proteins for isoprenylation and geranylgeranylation inhibitionReactant involved in· Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents· Double allylic alkylation of indole-2-hydroxamates· SN2 substitution reactions at amide nitrogens· Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines

IUPAC Name：O-tert-butylhydroxylamine;hydrochloride

INCHI：InChI=1S/C4H11NO.ClH/c1-4(2,3)6-5;/h5H2,1-3H3;1H

InChi Key：ZBDXGNXNXXPKJI-UHFFFAOYSA-N

Canonical SMILES：CC(C)(C)ON.Cl

Isomeric SMILES：CC(C)(C)ON.Cl

WGK Germany：3

PubChem CID：2777906

溶解性：可溶于水

敏感性：易吸湿

熔点：156 °C(dec.)

象形图：

信号词：Warning

危险声明：H315 Causes skin irritationH319 Causes serious eye irritation

预防措施声明：P305+P351+P338,P210,P362+P364,P332+P313

个人防护装备：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

产品包装