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1H-Indene-1-carboxylic acid, 2,3-dihydro-6-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

216582-47-7

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216582-47-7 Usage

Derivative of indene

bicyclic aromatic hydrocarbon
1H-Indene-1-carboxylic acid, 2,3-dihydro-6-hydroxyis derived from indene, which is a bicyclic (two fused rings) aromatic hydrocarbon.
3. Presence of carboxylic acid and hydroxyl group
The structure of the compound features a carboxylic acid (-COOH) and a hydroxyl (-OH) group, which contribute to its chemical properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 216582-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,5,8 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 216582-47:
(8*2)+(7*1)+(6*6)+(5*5)+(4*8)+(3*2)+(2*4)+(1*7)=137
137 % 10 = 7
So 216582-47-7 is a valid CAS Registry Number.

216582-47-7SDS

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 6-hydroxy-2,3-dihydro-1H-indene-1-carboxylic acid

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:216582-47-7 SDS

216582-47-7Relevant academic research and scientific papers

FARNESOID X RECEPTOR AGONISTS

-

, (2009/01/23)

The present invention relates to famesoid X receptors (FXR, NR1 H4) FXR is a member of the nuclear receptor class of ligand-activated transcription factors More particularly, the present invention relates to compounds useful as agonists for FXR, pharmaceu

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