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.
112448-60-9Relevant 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.