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6698-32-4

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6698-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6698-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,9 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6698-32:
(6*6)+(5*6)+(4*9)+(3*8)+(2*3)+(1*2)=134
134 % 10 = 4
So 6698-32-4 is a valid CAS Registry Number.

6698-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-hydroxy-6-methoxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names -

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:6698-32-4 SDS

6698-32-4Relevant articles and documents

Assignment of the absolute configuration of blasticidin A and revision of that of aflastatin A

Sakuda, Shohei,Matsumori, Nobuaki,Furihata, Kazuo,Nagasawa, Hiromichi

, p. 2527 - 2531 (2008/02/02)

The absolute configuration of blasticidin A, a strong inhibitor of aflatoxin production by Aspergillus parasiticus, was assigned by adding the data of relative configurations at its diol and pentaol moieties to previously known stereochemistry. Similarity

Regioselective acylation of carbohydrates with 1-acyloxy-1H-benzotriazoles

Pelyvas,Lindhorst,Streicher,Thiem

, p. 1015 - 1018 (2007/10/02)

Acylation of representative carbohydrate derivatives was accomplished with in situ generated 1-acyloxy-1H-benzotriazoles. The observed high regioselectivity, mild reaction conditions and convenient work-up make the presented one-pot procedure generally applicable and more advantageous than acylations with previously introduced reagents, including N-acylimidazoles.

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