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1579-15-3

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1579-15-3 Usage

Derivative of indenone

It is a modified version of indenone, which is a bicyclic organic compound.

Acetyloxy group attachment

The chemical has an acetyloxy group (-COCH3) attached to the second carbon atom.

Pharmaceutical production

The chemical is used in the manufacturing of various pharmaceuticals.

Dye production

It is also used in the synthesis of dyes.

Organic synthesis reactions

The compound is involved in various organic synthesis reactions.

Intermediate in synthesis

The chemical serves as an intermediate in the synthesis of various organic compounds, making it a valuable chemical in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1579-15-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1579-15:
(6*1)+(5*5)+(4*7)+(3*9)+(2*1)+(1*5)=93
93 % 10 = 3
So 1579-15-3 is a valid CAS Registry Number.

1579-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-oxo-1,2-dihydroinden-2-yl) acetate

1.2 Other means of identification

Product number -
Other names rac-2-acetoxyindanone

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:1579-15-3 SDS

1579-15-3Relevant articles and documents

Biocatalytic racemization of α-hydroxy ketones (acyloins) at physiological conditions using Lactobacillus paracasei DSM 20207

Nestl, Bettina M.,Kroutil, Wolfgang,Faber, Kurt

, p. 873 - 876 (2006)

Biocatalytic racemization of open-chain and cyclic dialkyl-, alkyl-aryl- and diaryl-substituted acyloins was accomplished using whole resting cells of Lactobacillus paracasei DSM 20207. The mild (physiological) reaction conditions ensured the suppression of undesired side reactions, such as elimination or condensation. This novel biocatalytic isomerization protocol represents an essential tool for the deracemization of pharmacologically important building blocks.

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