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Phenol, 4,6-dibromo-3-methoxy-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88010-47-3

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88010-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88010-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,1 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88010-47:
(7*8)+(6*8)+(5*0)+(4*1)+(3*0)+(2*4)+(1*7)=123
123 % 10 = 3
So 88010-47-3 is a valid CAS Registry Number.

88010-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dibromo-3-methoxy-2-methylphenol

1.2 Other means of identification

Product number -
Other names Phenol,4,6-dibromo-3-methoxy-2-methyl

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:88010-47-3 SDS

88010-47-3Relevant academic research and scientific papers

Antitumour indolequinones: Synthesis and activity against human pancreatic cancer cells

Inman, Martyn,Visconti, Andrea,Yan, Chao,Siegel, David,Ross, David,Moody, Christopher J.

, p. 4848 - 4861 (2014/07/07)

An important determinant of the growth inhibitory activity of indolequinones against pancreatic cancer cells is substitution on the 2-position with 2-unsubstituted derivatives being markedly more potent. A series of indolequinones bearing a range of subst

A Short, Convergent Synthesis of Aristolindiquinone

Botha, Marc E.,Giles, Robin G. F.,Yorke, Selwyn C.

, p. 85 - 88 (2007/10/02)

Aristolindiquinone, 2,5-dihydroxy-3,8-dimethyl-1,4-naphthoquinone 1, is synthesised by the regiochemical addition of 1-methoxy-1-trimethylsiloxypenta-1,3-diene 2 to 5-bromo-2-methoxy-3-methyl-1,4-benzoquinone 3.The regioisomer 2,8-dihydroxy-3,5-dimethyl-1

Regiospecific and highly stereoselective formation of benzisochroman-6,9-quinones. Synthesis of (±)-ventilagone and (±)-ventiloquinone H

Blouin,Beland,Brassard

, p. 1466 - 1471 (2007/10/02)

An approach known to give regiospecific cycloadditions over a wide range of substrates has been applied to the synthesis of (±)-ventilagone and (±)-ventiloquinone H using a novel, electron-rich heterocyclic diene. The strategy provides for the sole format

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