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5655-26-5

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5655-26-5 Usage

General Description

2-(chroman-4-yl)acetic acid is a chemical compound with a molecular formula of C11H10O3 and a molar mass of 190.2 g/mol. It is a carboxylic acid derivative with a chroman-4-yl group attached to the acetic acid moiety. 2-(chroman-4-yl)acetic acid has potential pharmacological properties and has been studied for its anti-inflammatory and immunomodulatory effects. It has been proposed as a potential therapeutic agent for various conditions, including autoimmune disorders and inflammatory diseases. The compound may also have applications in drug development and medicinal chemistry due to its unique structure and potential physiological effects. Overall, 2-(chroman-4-yl)acetic acid is a compound of interest for its potential therapeutic and pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5655-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5655-26:
(6*5)+(5*6)+(4*5)+(3*5)+(2*2)+(1*6)=105
105 % 10 = 5
So 5655-26-5 is a valid CAS Registry Number.

5655-26-5SDS

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 2-(3,4-dihydro-2H-chromen-4-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (chroman-4-yl)acetic acid

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:5655-26-5 SDS

5655-26-5Relevant articles and documents

Facile synthesis of 2,3-dihydrobenzofuran-3-ylacetic acids by novel electrochemical sequential aryl radical cyclization-carboxylation of 2-allyloxybromobenzenes using methyl 4-tert-butylbenzoate as an electron-transfer mediator

Senboku, Hisanori,Michinishi, Jun-Ya,Hara, Shoji

supporting information; experimental part, p. 1567 - 1572 (2011/08/03)

Facile synthesis of 2,3-dihydrobenzofuran-3-ylacetic acids and related analogues was successfully carried out by a novel electrochemical aryl radical generation and its 5-exo cyclization followed by a carboxylation sequence of 2-allyloxybromobenzenes by u

Synthesis and antiulcer activity of (isochroman-1-yl)alkylamines. II

Yamato,Hashigaki,Hitomi,Ishikawa

, p. 3453 - 3461 (2007/10/02)

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