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83983-71-5

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83983-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83983-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,8 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83983-71:
(7*8)+(6*3)+(5*9)+(4*8)+(3*3)+(2*7)+(1*1)=175
175 % 10 = 5
So 83983-71-5 is a valid CAS Registry Number.

83983-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-2,3-dihydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 6-Brom-2,3-dihydroxybenzaldehyd

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:83983-71-5 SDS

83983-71-5Relevant articles and documents

Enantioselective Alkynylation of Trifluoromethyl Ketones Catalyzed by Cation-Binding Salen Nickel Complexes

Park, Dongseong,Jette, Carina I.,Kim, Jiyun,Jung, Woo-Ok,Lee, Yongmin,Park, Jongwoo,Kang, Seungyoon,Han, Min Su,Stoltz, Brian M.,Hong, Sukwon

supporting information, p. 775 - 779 (2019/12/24)

Cation-binding salen nickel catalysts were developed for the enantioselective alkynylation of trifluoromethyl ketones in high yield (up to 99 %) and high enantioselectivity (up to 97 % ee). The reaction proceeds with substoichiometric quantities of base (

Method for synthesizing natural product salvianolic acid A methyl ester

-

, (2017/07/20)

The invention relates to a novel method for synthesizing natural product salvianolic acid A methyl ester. A synthetic route is unique and novel in design; key strategies and steps comprise the step of using an easily-removed t-butyldimethylsilyl protectin

CYSTOBACTAMIDES

-

Paragraph 0393; 0394; 0395; 0396, (2016/06/13)

The present invention provides cystobactamides of formula (I) and the use thereof for the treatment or prophylaxis of bacterial infections:

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