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82040-74-2

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82040-74-2 Usage

Type of compound

Nitroaromatic compound

Structural features

Bromine atom
Two methoxy groups
Benzene ring
(E)-2-nitroethenyl group

Uses

Precursor in the synthesis of pharmaceuticals
Precursor in the synthesis of organic compounds
Potential building block for new materials and research chemicals

Physical state

Yellow crystalline solid

Molecular weight

289.10 g/mol

Hazard classification

Hazardous material

Safety measures

Special handling and storage precautions required

Potential risks

Toxicity and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 82040-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,4 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82040-74:
(7*8)+(6*2)+(5*0)+(4*4)+(3*0)+(2*7)+(1*4)=102
102 % 10 = 2
So 82040-74-2 is a valid CAS Registry Number.

82040-74-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4,5-dimethoxy-2-[(E)-2-nitroethenyl]benzene

1.2 Other means of identification

Product number -
Other names Benzene,5-dimethoxy-2-(2-nitroethenyl)-,(E)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82040-74-2 SDS

82040-74-2Relevant articles and documents

Synthesis of 3-arylindole derivatives from nitroalkane precursors

Huang, Chia-Yu,Kuo, Chun-Wei,Konala, Ashok,Yang, Tang-Hao,Lin, Lyu,Chen, Yu-Wen,Kavala, Veerababurao,Yao, Ching-Fa

, p. 96049 - 96056 (2016/10/25)

3-Arylindole derivatives were synthesized by Cu(i) catalysed intramolecular Ullmann coupling of 2-bromoarylaminoalkanes. 2-Bromoarylaminoalkanes were synthesized from 2-bromoarylnitroalkanes, which in turn prepared through AlCl3-mediated Friede

An intramolecular aryne cycloaddition approach to phenanthrene alkaloids

Estevez,Estevez,Castedo

, p. 6883 - 6884 (2007/10/02)

A new synthesis of phenanthrene alkaloids which is based on the intramolecular Diels-Alder reaction between a styrene and an aryne is described.

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