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88040-04-4

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88040-04-4 Usage

Chiral molecule

It has a non-superimposable mirror image, making it an enantiomer

Uses in pharmaceutical industry

Potential therapeutic agent for neurological disorders, cancer, and inflammatory diseases

Properties

Known for antioxidant and anti-inflammatory properties

Potential in drug development

Research indicates potential for developing new drugs for various health conditions

Need for further research

More research is needed to fully understand its potential uses and effects

Check Digit Verification of cas no

The CAS Registry Mumber 88040-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,4 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88040-04:
(7*8)+(6*8)+(5*0)+(4*4)+(3*0)+(2*0)+(1*4)=124
124 % 10 = 4
So 88040-04-4 is a valid CAS Registry Number.

88040-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Phenyl-6-chromanol

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:88040-04-4 SDS

88040-04-4Upstream product

88040-04-4Downstream Products

88040-04-4Relevant articles and documents

TRANSFORMATION DU CATION ISOFLAVYLIUM EN PHENYL-3 COUMARINES, ISOFLAVENES-3 ET ISOFLAVANNES

Deschamps-Vallet, Colette,Ilotse, Jean-Baptiste,Meyer-Dayan, Michele

, p. 3993 - 3996 (2007/10/02)

Isoflavylium salts 1 are key starting materials for synthesis of 3-phenyl coumarins 2,isoflav-3-enes 4 and isoflavans 5, by chemical conversions narrowsly apparented to biogenetic pathways actually recognized for natural compounds of these series.

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