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2-(2,4,6-trimethyl-3-oxo-2,3-dihydro-1H-inden-5-yl)ethyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39815-61-7

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39815-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39815-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,1 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39815-61:
(7*3)+(6*9)+(5*8)+(4*1)+(3*5)+(2*6)+(1*1)=147
147 % 10 = 7
So 39815-61-7 is a valid CAS Registry Number.

39815-61-7SDS

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 (2R)-Benzoylpterosin B

1.2 Other means of identification

Product number -
Other names Benzoic acid 2-((R)-2,4,6-trimethyl-3-oxo-indan-5-yl)-ethyl ester

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:39815-61-7 SDS

39815-61-7Downstream Products

39815-61-7Relevant academic research and scientific papers

A concise stereoselective synthesis of pterosin B

Dexter, Hannah R.,Allen, Esther,Williams, David M.

, p. 4323 - 4325 (2018)

Pterosin B is a naturally occurring indanone found in bracken fern (Pteridium aquilinum) that displays a variety of interesting pharmacological properties, but for which few stereoselective syntheses exist. Herein we describe a 7-step stereoselective synthesis of (2R)-pterosin B via 6-bromo-5,7-dimethylindan-1-one whose structure was confirmed by NOE analysis and structure determination by X-ray crystallography. The hydroxyethyl chain was introduced via a Suzuki-Miyaura cross-coupling reaction. The 2-methyl group was introduced stereoselectively by methylation of a SAMP [(S)-1-amino-2-methoxymethyl)pyrrolidine] hydrazone and the chiral auxiliary was removed to produce (2R)-pterosin B. The structure of pterosin B was confirmed by specific rotation and structural determination by X-ray crystallography.

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