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7-HYDROXY-3-PHENYL-2-TRIFLUOROMETHYL-CHROMEN-4-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84858-65-1

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84858-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84858-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,5 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84858-65:
(7*8)+(6*4)+(5*8)+(4*5)+(3*8)+(2*6)+(1*5)=181
181 % 10 = 1
So 84858-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H9F3O3/c17-16(18,19)15-13(9-4-2-1-3-5-9)14(21)11-7-6-10(20)8-12(11)22-15/h1-8,20H

84858-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-hydroxy-3-phenyl-2-(trifluoromethyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names 7-hydroxy-2-trifluoromethylisoflavone

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:84858-65-1 SDS

84858-65-1Relevant academic research and scientific papers

COMPOUNDS FOR IMMUNOPOTENTIATION

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Page/Page column 112, (2010/02/15)

Methods of stimulating an immune response and treating patients responsive thereto with 3,4-di(1H-indol-3-yl)-1H-pyrrole-2,5-diones, staurosporine analogs, derivatized pyridazines, chromen-4-ones, indolinones, quinazolines, nucleoside analogs, and other small molecules are disclosed.

Flavones. 3. Synthesis, biological activities, and conformational analysis of isoflavone derivatives and related compounds

Wu,Loch III,Toder,Borrelli,Gawlak,Radov,Gensmantel

, p. 3519 - 3525 (2007/10/02)

A series of 2-alkylisoflavone derivatives 1 was prepared with the intent to study the importance of the phenyl group (at the 3-position) of the isoflavone in imparting antihypertensive activity and the substitution effects at the 2-position of isoflavone.

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