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Merck
CN

125911

Sigma-Aldrich

α,α′-二溴-间二甲苯

greener alternative

97%

别名:

1,3-二(溴甲基)苯, 二溴间二甲苯

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About This Item

线性分子式:
C6H4(CH2Br)2
CAS号:
分子量:
263.96
Beilstein:
971085
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

表单

solid

环保替代产品得分

old score: 10
new score: 6
Find out more about DOZN™ Scoring

环保替代产品特性

Waste Prevention
Atom Economy
Safer Solvents and Auxiliaries
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

沸点

135-140 °C/20 mmHg (lit.)

mp

74-77 °C (lit.)

官能团

bromo

环保替代产品分类

SMILES字符串

BrCc1cccc(CBr)c1

InChI

1S/C8H8Br2/c9-5-7-2-1-3-8(4-7)6-10/h1-4H,5-6H2

InChI key

OXHOPZLBSSTTBU-UHFFFAOYSA-N

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一般描述

α,α′-二溴--二甲苯可交联并环化含有两个半胱氨酸残基的肽
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives. This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Waste Prevention”, “Atom Economy” and “Safer Solvents and Auxiliaries”. Click here to view its DOZN scorecard.

应用

α,α′-二溴--二甲苯已被用于以 -和 二甲苯桥作为新茂金属化合物的四种新型双核半钛合金的制备 。它被用于不对称 大环盐的合成

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Preparation of new dinuclear half-titanocene complexes with ortho- and meta-xylene linkages and investigation of styrene polymerization.
Linh NTB, et al.
Journal of Organometallic Chemistry, 694(21), 3438-3443 (2009)
Florian P Seebeck et al.
Journal of the American Chemical Society, 128(22), 7150-7151 (2006-06-01)
Dehydroalanine is a nonproteinogenic amino acid, but it is a component of a wide variety of natural products with therapeutic activities. Indeed, this alpha,beta-unsaturated residue is a highly versatile building block due to its rigidifying effect on peptide backbones and
Bis-aminals: efficient tools for bis-macrocycle synthesis.
Le Baccon M, et al.
New. J. Chem., 25(9), 1168-1174 (2001)

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