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885519-07-3

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885519-07-3 Usage

General Description

4-Bromo-2-methoxy-6-nitrotoluene is a chemical compound with the molecular formula C7H7BrNO3. It is a nitroaromatic compound that is used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It is a yellow solid with a slight odor and is insoluble in water but soluble in organic solvents. This chemical is mainly used as an intermediate in the production of other chemicals and is also utilized in research and development processes. It is important to handle this compound with care, as it may be harmful if ingested, inhaled, or comes into contact with the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 885519-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,5,1 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 885519-07:
(8*8)+(7*8)+(6*5)+(5*5)+(4*1)+(3*9)+(2*0)+(1*7)=213
213 % 10 = 3
So 885519-07-3 is a valid CAS Registry Number.

885519-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-1-methoxy-2-methyl-3-nitrobenzene

1.2 Other means of identification

Product number -
Other names 4-Bromo-2-methoxy-6-nitrotoluene

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:885519-07-3 SDS

885519-07-3Relevant articles and documents

A Concise Total Synthesis of Breitfussin A and B

Pandey, Sunil Kumar,Guttormsen, Yngve,Haug, Bengt Erik,Hedberg, Christian,Bayer, Annette

, p. 122 - 125 (2015/07/28)

(Chemical Equation Presented). The first total synthesis of breitfussin A and B is described. The approach features two palladium-catalyzed cross-couplings installing the indole and pyrrole onto the oxazole core and selective lithiation/iodination of a common indole-oxazole fragment providing 2,4-diiodinated or 2-iodinated oxazoles as potential precursors for breitfussin A and B, respectively. An unexpected acid promoted deiodination was utilized in the synthesis of breitfussin B. Comparison of the synthetic material with previously reported spectral data of isolated breitfussin A and B verified the structure of the breitfussin framework.

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