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36942-56-0

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36942-56-0 Usage

Chemical Properties

Pale yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 36942-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,4 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36942-56:
(7*3)+(6*6)+(5*9)+(4*4)+(3*2)+(2*5)+(1*6)=140
140 % 10 = 0
So 36942-56-0 is a valid CAS Registry Number.

36942-56-0SDS

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 2-Bromo-4-methoxy-1-methylbenzene

1.2 Other means of identification

Product number -
Other names 2-Bromo-4-methoxytoluene

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:36942-56-0 SDS

36942-56-0Relevant articles and documents

Magnolol dimer-derived fragments as PPARγ-selective probes

Dreier, Dominik,Resetar, Mirta,Temml, Veronika,Rycek, Lukas,Kratena, Nicolas,Schnürch, Michael,Schuster, Daniela,Dirsch, Verena M.,Mihovilovic, Marko D.

, p. 7019 - 7028 (2018)

Partial agonists of the transcription factor PPARγ (peroxisome proliferator-activated receptor γ) have shown potential for the treatment of metabolic and inflammatory conditions and novel activators serve as valuable tool and lead compounds. Based on the

ENANTIOPURE TERPHENYLS WITH TWO ORTHO-ATROPISOMERIC AXES

-

Page/Page column 18-19, (2019/07/19)

Enantiopure terphenyl presenting two ortho-located chiral axes having the following structural formula (I) : their process of synthesis and their use as mono or bidentate ligands for asymmetric organometallic reactions, as organocatalysts, as chiral base

Fast and Tight Boronate Formation for Click Bioorthogonal Conjugation

Akgun, Burcin,Hall, Dennis G.

supporting information, p. 3909 - 3913 (2016/03/19)

A new click bioorthogonal reaction system was devised to enable the fast ligation (kON≈340 m-1 s-1) of conjugatable derivatives of a rigid cyclic diol (nopoldiol) and a carefully optimized boronic acid partner, 2-methyl-5-carboxymethylphenylboronic acid. Using NMR and fluorescence spectroscopy studies, the corresponding boronates were found to form reversibly within minutes at low micromolar concentration in water, providing submicromolar equilibrium constant (Keq≈105-106 m-1). Efficient protein conjugation under physiological conditions was demonstrated with model proteins thioredoxin and albumin, and characterized by mass spectrometry and gel electrophoresis.

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