90435-23-7 Usage
Uses
Used in Food Industry:
Butanoic acid, 3-hydroxy-, 1,1-dimethylethyl ester is used as a flavoring agent for its fruity odor, enhancing the taste and aroma of various food products.
Used in Perfumes and Cosmetics:
Butanoic acid, 3-hydroxy-, 1,1-dimethylethyl ester is used as a fragrance ingredient in perfumes and cosmetics, providing a pleasant and fruity scent.
Used in Plastics Production:
Butanoic acid, 3-hydroxy-, 1,1-dimethylethyl ester is used in the production of plastics, contributing to the development of various plastic materials.
Used in Pharmaceutical Industry:
Butanoic acid, 3-hydroxy-, 1,1-dimethylethyl ester is used in the pharmaceutical industry, potentially for the synthesis of drugs or as a solvent in drug formulations.
Used as a Solvent in Industrial Applications:
Butanoic acid, 3-hydroxy-, 1,1-dimethylethyl ester is used as a solvent in various industrial applications, such as in the manufacturing process of different products.
It is important to handle and store Butanoic acid, 3-hydroxy-, 1,1-dimethylethyl ester with proper safety precautions due to its potential flammability and irritant properties.
Check Digit Verification of cas no
The CAS Registry Mumber 90435-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,3 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90435-23:
(7*9)+(6*0)+(5*4)+(4*3)+(3*5)+(2*2)+(1*3)=117
117 % 10 = 7
So 90435-23-7 is a valid CAS Registry Number.
90435-23-7Relevant academic research and scientific papers
Bonini, Carlo,Fabio, Romano Di
, p. 819 - 822 (1988)
A free radical reaction has been applied to several 1,2 epoxides; the regio and chemoselective reduction of the epoxy ring to afford secondary alcohols occours, in presence of NaI and nBu3SnH in DME at 80 deg C, in rather good yield.
Process for preparing optically active 3-azidocarboxylic acid derivatives and 3-aminocarboxylic acid derivatives
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Page/Page column 9, (2008/06/13)
A process for enantioselectively preparing 3-azidocarboxylic acid derivatives comprises reacting 3-sulfonatocarboxylic acid derivatives with an alkali metal azide in a solvent selected from the group comprising certain carboxamides; a solvent mixture which comprises such carboxamides; a solvent mixture of water and a solvent miscible homogeneously with water; water with the proviso that the addition of a phase transfer catalyst is not used in the reaction in water; and DMSO. The resulting products are optionally reduced to 3-aminocarboxylic acid derivatives.
