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1-oxo-2-phenyl-1H-inden-3-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1953-70-4

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1953-70-4 Usage

Classification

Acetone derivative it is an acetate ester of 1-oxo-2-phenyl-1H-inden-3-yl, which is a type of chemical compound derived from ketones.

Usage in industries

Pharmaceutical and fragrance industries the compound is commonly used in these industries due to its unique properties and potential applications.

Odor

Aromatic and slightly sweet this characteristic odor makes it a popular choice for use in perfumes and other scented products.

Potential applications

Synthesis of organic compounds the unique structure and reactivity of 1-oxo-2-phenyl-1H-inden-3-yl acetate allow it to be used in the synthesis of various organic compounds.

Biological activity

Area of interest in medicinal chemistry the compound may exhibit biological activity, making it a subject of research in the field of medicinal chemistry.

Versatility

Various industrial and scientific applications 1-oxo-2-phenyl-1H-inden-3-yl acetate has a wide range of potential uses, making it a valuable compound in both industrial and scientific settings.

Check Digit Verification of cas no

The CAS Registry Mumber 1953-70-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1953-70:
(6*1)+(5*9)+(4*5)+(3*3)+(2*7)+(1*0)=94
94 % 10 = 4
So 1953-70-4 is a valid CAS Registry Number.

1953-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-oxo-2-phenylinden-1-yl) acetate

1.2 Other means of identification

Product number -
Other names 1-oxo-2-phenyl-1h-inden-3-yl acetate

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:1953-70-4 SDS

1953-70-4Relevant academic research and scientific papers

SYNTHESIS AND PROPERTIES OF ESTERS OF 3-HYDROXY-2-PHENYLINDEN-1-ONE, 2-HYDROXYMETHYL-2-PHENYL-1,3-INDANEDIONE, AND CARBOXYLIC AND CARBONIC ACIDS

Marshalkin, V. N.,Smirnova, T. V.

, p. 339 - 345 (2007/10/02)

The O-acylation of 2-phenyl-1,3-indanedione by carboxylic acid chlorides and chloroformates was realized in the presence of triethylamine.Growth-regulating activity was found in the obtained esters.The acylation of 2-hydroxymethyl-2-phenyl-1,3-indanedione by carboxylic acid chlorides was investigated in the presence of triethylamine.It was established that the reaction is unsuitable for the production of 2-acyloxymethyl-2-phenyl-1,3-indanediones.A method is proposed for the synthesis of these esters by the reaction of 2-iodomethyl-2-phenyl-1,3-indanedione with the potassium salts of carboxylic acids under the conditions of phase-transfer catalysis.

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