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288399-90-6

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288399-90-6 Usage

Chemical compound

6-FLUORO-4-METHYLCOUMARIN-3-CARBONITRIL

Family

Coumarin

Functional groups

Fluorine atom, methyl group, carbonitrile

Uses

starting material for synthesis of pharmaceuticals, agrochemicals, fine chemicals

Biological activities

anticancer, anti-inflammatory, antimicrobial

Applications

drug discovery, development, materials science, fluorescent probe in analytical chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 288399-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,3,9 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 288399-90:
(8*2)+(7*8)+(6*8)+(5*3)+(4*9)+(3*9)+(2*9)+(1*0)=216
216 % 10 = 6
So 288399-90-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H6FNO2/c1-6-8-4-7(12)2-3-10(8)15-11(14)9(6)5-13/h2-4H,1H3

288399-90-6 Well-known Company Product Price

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  • Aldrich

  • (543713)  6-Fluoro-4-methylcoumarin-3-carbonitrile  97%

  • 288399-90-6

  • 543713-1G

  • 1,083.42CNY

  • Detail

288399-90-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoro-4-methyl-2-oxochromene-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-Cyano-6-fluoro-4-methylcoumarin

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:288399-90-6 SDS

288399-90-6Downstream Products

288399-90-6Relevant articles and documents

Iridium-catalyzed direct asymmetric vinylogous allylic alkylation

Shi, Chang-Yun,Xiao, Jun-Zhao,Yin, Liang

supporting information, p. 11957 - 11960 (2018/11/02)

The catalytic asymmetric vinylogous allylic alkylation of α,β-unsaturated lactones (including coumarins) was achieved with excellent regio- and enantioselectivity. Transformations of the product were carried out by means of the versatile terminal olefin and lactone moieties. The synthetic application of the present methodology was showcased by the asymmetric synthesis of an advanced synthetic Merck intermediate toward a new drug candidate.

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