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31804-36-1

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31804-36-1 Usage

General Description

1-Bromo-3-methoxy-2-methylbenzene, also known as o-bromoanisole or 3-bromoanisole, is an organic compound with the formula C8H9BrO. 1-BROMO-3-METHOXY-2-METHYLBENZENE belongs to the family of bromobenzenes, and specifically can be classified as a bromoanisole. It is a light yellow to amber liquid and has a molecular weight of 201.06 g/mol. It is typically used in laboratory settings for organic synthesis. Like all bromobenzenes, 1-Bromo-3-methoxy-2-methylbenzene is relatively nonpolar and thus insoluble in water but soluble in organic solvents. The handling and storage of this chemical should be done with caution as it can be harmful if swallowed, inhaled, or comes in contact with skin. It plays a significant role in the manufacturing of dyes, pharmaceuticals, and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 31804-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,8,0 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31804-36:
(7*3)+(6*1)+(5*8)+(4*0)+(3*4)+(2*3)+(1*6)=91
91 % 10 = 1
So 31804-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9BrO/c1-6-7(9)4-3-5-8(6)10-2/h3-5H,1-2H3

31804-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-3-methoxy-2-methylbenzene

1.2 Other means of identification

Product number -
Other names 2-methyl-3-bromoanisole

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:31804-36-1 SDS

31804-36-1Relevant articles and documents

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Cross,B.E.,Melvin,P.H.

, p. 3038 - 3040 (1960)

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Total Synthesis of (Nor)illudalane Sesquiterpenes Based on a C(sp3)-H Activation Strategy

Melot, Romain,Craveiro, Marcus V.,Baudoin, Olivier

, p. 12933 - 12945 (2019/08/20)

Three (nor)illudalane sesquiterpenes were synthesized from a common intermediate in racemic and enantioenriched forms using Pd0-catalyzed C(sp3)-H arylation as a key step. The configuration of the isolated, highly symmetric quaternar

Propionic Acid Derivatives and Methods of Use Thereof

-

, (2018/11/21)

Provided herein are compounds and pharmaceutical compositions of formula I where R1, R2, R3, R4, R5 and R6 are as described herein. Also provided pharmaceutically acceptable salts or stereoisomers of these compounds. In addition methods are provided for inhibiting the binding of an integrin to treat various pathophysiological conditions.

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