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Benzoic acid, 6-bromo-2,3,4-trimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139214-72-5

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139214-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139214-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,1 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 139214-72:
(8*1)+(7*3)+(6*9)+(5*2)+(4*1)+(3*4)+(2*7)+(1*2)=125
125 % 10 = 5
So 139214-72-5 is a valid CAS Registry Number.

139214-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-2,3,4-trimethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,6-bromo-2,3,4-trimethoxy

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:139214-72-5 SDS

139214-72-5Downstream Products

139214-72-5Relevant academic research and scientific papers

A short total synthesis of the alkaloids piperolactam C, goniopedaline, and stigmalactam

Rys, Veronique,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre

, p. 1231 - 1237 (2007/10/03)

The total synthesis of the polyalkoxylated alkaloids piperolactam C, goniopedaline and stigmalactam by combinatorial metalation/cyclization strategies has been achieved. The synthetic route involved the preliminary construction of the polyalkoxylated isoindolinone template by Parham's technique. Benzylic lactam deprotonation allowed connection of a hydroxybenzyl appendage, and the synthesis of the target natural products was completed by subsequent E1cB elimination, radical cyclization and final deprotection. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

On the Synthesis of a Phenanthrene-2,7-quinone

Hewgill, Frank R.,Slamet, Riskiono,Stewart, Jeffery M.

, p. 3033 - 3042 (2007/10/02)

Oxidative coupling of 2,2',4,4'-tetramethoxystilbene-3,3'-diol 51 gave a 51percent yield of 1,3,6,8-tetramethoxyphenanthrene-2,7-quinone 52, the first isolated example of a quinone of this type.Similar oxidation of the corresponding diphenylethane 55 gave

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