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13206-55-8

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13206-55-8 Usage

Class

Indenols

Physical form

White to light yellow crystalline powder

Molecular weight

238.333 g/mol

Uses

Building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals; production of fragrances and flavoring agents

Biological activities

Potential anti-inflammatory and anticancer properties.

Check Digit Verification of cas no

The CAS Registry Mumber 13206-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,0 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13206-55:
(7*1)+(6*3)+(5*2)+(4*0)+(3*6)+(2*5)+(1*5)=68
68 % 10 = 8
So 13206-55-8 is a valid CAS Registry Number.

13206-55-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2R)-2-phenylsulfanyl-2,3-dihydro-1H-inden-1-ol

1.2 Other means of identification

Product number -
Other names cis-2-Phenylmercaptoindanol

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:13206-55-8 SDS

13206-55-8Relevant articles and documents

Chemoenzymatic synthesis of enantiopure hydroxy sulfoxides derived from substituted arenes

Boyd, Derek R.,Sharma, Narain D.,Malone, John F.,Ljubez, Vera,Murphy, Deirdre,Shepherd, Steven D.,Allen, Christopher C. R.

, p. 2651 - 2664 (2016/03/05)

Enantiopure β-hydroxy sulfoxides and catechol sulfoxides were obtained, by chemoenzymatic synthesis, involving dioxygenase-catalysed benzylic hydroxylation or arene cis-dihydroxylation and cis-diol dehydrogenase-catalysed dehydrogenation. Absolute configurations of chiral hydroxy sulfoxides were determined by X-ray crystallography, ECD spectroscopy and stereochemical correlation. The application of a new range of β-hydroxy sulfoxides as chiral ligands was examined.

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