主要文件

查看所有文档

136727

3-氯苄溴

Name: 3-氯苄溴
Brand: ALDRICH

97%

别名:

α-溴-3-氯甲苯

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:

ClC₆H₄CH₂Br

化学文摘社编号:

766-80-3

分子量:

205.48

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24848293

EC Number:

212-171-0

Beilstein/REAXYS Number:

636504

MDL number:

MFCD00000597

Assay:

97%

Form:

liquid

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.588 (lit.)

bp

109-110 °C/12 mmHg (lit.)

density

1.565 g/mL at 25 °C (lit.)

functional group

bromo, chloro

SMILES string

Clc1cccc(CBr)c1

InChI

1S/C7H6BrCl/c8-5-6-2-1-3-7(9)4-6/h1-4H,5H2

InChI key

LZIYAIRGDHSVED-UHFFFAOYSA-N

说明

General description

3-Chlorobenzyl bromide reacts with aminoethanol and NaH to yield aminoethyl 3-chlorobenzyl ether.

Application

3-Chlorobenzyl bromide was used in the synthesis of symmetrical and unsymmetrical benzyl thioethers. It was used as starting reagent during the synthesis of 1-(3-chlorobenzyl)-2-(pyrrolidin-1-ylmethyl)-1H-benzimidazole dihydrochloride.

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405

Hazard Classifications

Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

新产品

此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Selective inactivation of monoamine oxidase B by aminoethyl 3-chlorobenzyl ether.

Ding CZ and Silverman RB.

Bioorganic & Medicinal Chemistry, 3(10), 2077-2078 (1993)

Convenient and robust one-pot synthesis of symmetrical and unsymmetrical benzyl thioethers from benzyl halides using thiourea.

Eccles KS, et al.

ARKIVOC (Gainesville, FL, United States), ix, 216-218 (2010)

Selective inhibition of heme oxygenase-2 activity by analogs of 1-(4-chlorobenzyl)-2-(pyrrolidin-1-ylmethyl)-1H-benzimidazole (clemizole): Exploration of the effects of substituents at the N-1 position.

Jason Z Vlahakis et al.

Bioorganic & medicinal chemistry, 21(21), 6788-6795 (2013-09-12)

Several analogs based on the lead structure of 1-(4-chlorobenzyl)-2-(pyrrolidin-1-ylmethyl)-1H-benzimidazole (clemizole) were synthesized and evaluated as novel inhibitors of heme oxygenase (HO). Many of the compounds were found to be potent and highly selective for the HO-2 isozyme (constitutive), and had

全球贸易项目编号

货号	GTIN
136727-50G	04061837082719
136727-10G	04061837070877