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2,3-Butanediol, 2,3-dimethyl-1,4-diphenyl-, also known as a butanediol derivative, is a colorless liquid with a pleasant odor. It is a versatile chemical compound that belongs to the family of butanediols and has a wide range of industrial applications.

62640-71-5

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62640-71-5 Usage

Uses

Used in Plastics and Solvents Industry:
2,3-Butanediol, 2,3-dimethyl-1,4-diphenylis used as a solvent and a building block in the production of plastics and solvents. Its properties make it suitable for use in the manufacturing process, contributing to the desired characteristics of the final products.
Used in Dyes and Pharmaceuticals Manufacturing:
In the dyes and pharmaceuticals industry, 2,3-Butanediol, 2,3-dimethyl-1,4-diphenylis used as a solvent. Its ability to dissolve various substances makes it an essential component in the manufacturing process of dyes and pharmaceuticals, ensuring the proper formation and effectiveness of these products.
Used in Fragrances and Flavors Synthesis:
2,3-Butanediol, 2,3-dimethyl-1,4-diphenylis used as a precursor in the synthesis of fragrances and flavors. Its chemical structure allows for the creation of a variety of scent and taste profiles, making it a valuable component in the development of new fragrances and flavors.
Used in Polyesters and Polyurethanes Production:
As a building block, 2,3-Butanediol, 2,3-dimethyl-1,4-diphenylis used in the production of polyesters and polyurethanes. Its presence in the manufacturing process contributes to the formation of these polymers, which are widely used in various industries, including textiles, coatings, and adhesives.
Used in Medicinal and Therapeutic Applications:
2,3-Butanediol, 2,3-dimethyl-1,4-diphenylhas potential medicinal and therapeutic uses, particularly in the treatment of cardiovascular and neurodegenerative diseases. Its unique chemical properties may offer new avenues for the development of treatments and therapies for these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 62640-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,4 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62640-71:
(7*6)+(6*2)+(5*6)+(4*4)+(3*0)+(2*7)+(1*1)=115
115 % 10 = 5
So 62640-71-5 is a valid CAS Registry Number.

62640-71-5SDS

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 2,3-dimethyl-1,4-diphenylbutane-2,3-diol

1.2 Other means of identification

Product number -
Other names 2,3-Butanediol,2,3-dimethyl-1,4-diphenyl

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:62640-71-5 SDS

62640-71-5Relevant academic research and scientific papers

A new preparation of samarium dibromide and its use in stoichiometric and catalytic pinacol coupling reactions

Hélion, Florence,Lannou, Marie-Isabelle,Namy, Jean-Louis

, p. 5507 - 5510 (2007/10/03)

A new convenient preparation of samarium dibromide in THF is reported. Pinacol coupling reactions using SmBr2 in catalytic amounts together with mischmetall as a coreductant have been performed with a variety of carbonyl compounds.

Intramolecular Oxidative Coupling of Aromatic Compounds. V. para-para Diphenolic Oxidative Coupling as a Possible Route to the Eupodienone Skeleton

Carroll, Anthony R.,Krauss, Adrian S.,Taylor, Walter C.

, p. 277 - 292 (2007/10/02)

The synthesis of (2RS,3RS)-1,4-bis(4-hydroxy-3,5-dimethoxyphenyl)-2,3-dimethylbutan-1-one (9) is described.Diphenolic oxidative coupling of (9) gave the unstable dienone (24), which decomposed in methanol to give what is believed to be the acetal (26).Syn

Photochemistry of α-Aryl Carbonyl Compounds in Aqueous Solution

Wan, Peter,Yates, Keith

, p. 275 - 276 (2007/10/02)

Irradiation of the α-aryl carbonyl compounds (1) - (4) with u.v. light in aqueous solution gave different results from those observed in organic solvents.

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