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117211-16-2

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117211-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117211-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,2,1 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 117211-16:
(8*1)+(7*1)+(6*7)+(5*2)+(4*1)+(3*1)+(2*1)+(1*6)=82
82 % 10 = 2
So 117211-16-2 is a valid CAS Registry Number.

117211-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-(2-hydroxy-3-methoxyphenyl)-7-methyl-7,8-dihydro-6H-[1,3]dioxolo[4,5-g]chromen-6-ol

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:117211-16-2 SDS

117211-16-2Downstream Products

117211-16-2Relevant articles and documents

New Anti-tumor Agents. 2. Benzopyranylamine Compounds

Jurd, Leonard

, p. 1919 - 1925 (2007/10/03)

Pyrrolidine, morpholine and piperidine derived Mannich bases of types 1-3 react with acetone, propionaldehyde and butyraldehyde to form 2-methyl and 3-methylbenzopyrans of types 4-8. Hydrolysis of these benzopyrans yields alcoholic benzopyrans which readily condense with a variety of amine, aniline and hydrazine derivatives to form diverse isomeric benzopyrans of types of 9 and 10. The benzopyrans 4-9 which contain a 3,4,5-trimethoxyphenyl ring are active anti-tumor agents, particularly against human breast, CNS and colon cancer cell lines, total growth inhibition of these tumors often occurring in vitro at concentrations as low as 10-5-10-6 moles/l. Because of their in vitro activities and unusual structures a number of these benzopyrans have been selected for in vivo Xenograft testing against breast and other susceptible human cancers.

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