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112448-60-9

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112448-60-9 Usage

Explanation

The full name of the compound, which describes its structure and stereochemistry.

Explanation

The compound is derived from 1,4-Butanediol, a solvent and precursor in the production of plastics and textiles.

Explanation

The 2,3-bis(1,3-benzodioxol-5-ylmethyl)compound is known for its potential use as a precursor in the synthesis of pharmaceuticals and other organic compounds.

Explanation

The compound contains an acetate functional group, which can have various chemical and biological properties.

Explanation

The stereochemistry designation (2R,3R) indicates the arrangement of the atoms in the molecule, which can impact its reactivity and biological activity.

Explanation

The compound has potential applications in the pharmaceutical and chemical industries due to its unique structure and properties.

Explanation

The precise structure and properties of the compound make it an interesting target for further research and development in various fields.

Derived from

1,4-Butanediol

Potential use

Pharmaceutical synthesis

Functional group

1-acetate

Stereochemistry

(2R,3R)

Applications

Pharmaceutical and chemical industries

Research and development

Interesting target

Check Digit Verification of cas no

The CAS Registry Mumber 112448-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112448-60:
(8*1)+(7*1)+(6*2)+(5*4)+(4*4)+(3*8)+(2*6)+(1*0)=99
99 % 10 = 9
So 112448-60-9 is a valid CAS Registry Number.

112448-60-9SDS

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 threo-(-)-2,3-bis(3',4'-methylenedioxybenzyl)-1,4-butanediol monoacetate

1.2 Other means of identification

Product number -
Other names hemiariensin

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:112448-60-9 SDS

112448-60-9Upstream product

112448-60-9Downstream Products

112448-60-9Relevant articles and documents

Lipase-catalyzed esterification of a (±)-2,3-di(arylmethyl)-1,4- butanediol and its application to the synthesis of (S,S)-(+)-hinokinin

Morimoto, Toshiaki,Nagai, Hazuki,Achiwa, Kazuo

, p. 857 - 865 (2007/10/03)

Racemic trans-2,3-di[(3,4-methylenedioxy)benzyl]-1,4-butanediol (dihydrocubebin) 6 was enantioselectively esterified using lipases as catalysts with vinyl acetate. Optically active (S,S)-1,4-butanediol 6 obtained was selectively oxygenated with a Fetizon reagent, affording (S,S)-(+)-hinokinin 9 in a high yield.

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