24562-96-7 Usage
Stereoisomer of 1,4-butanediol
Yes
It shares the same molecular formula as 1,4-butanediol but has a different arrangement of atoms in space.
Common use
Production of plastics, solvents, and pharmaceuticals
The compound has a wide range of applications in various industries due to its versatile chemical properties.
Organic compound
Yes
It is a carbon-containing compound, which classifies it as an organic compound.
Contains two benzodioxol groups
Yes
These groups are commonly found in drugs such as MDMA and contribute to the compound's unique properties.
Chiral molecule
Yes
The compound has a non-superimposable mirror image, making it a chiral molecule.
Enantiomers
(2R,3S)-reland its mirror image
The compound has two enantiomers, which are the (2R,3S)-relform and its mirror image.
Potential applications
Pharmaceutical synthesis and drug development
Due to its unique chemical structure, the compound has potential uses in creating new pharmaceuticals and drugs.
Unique chemical structure
Yes
The presence of benzodioxol groups and the chiral nature of the molecule contribute to its unique chemical structure.
Check Digit Verification of cas no
The CAS Registry Mumber 24562-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,6 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24562-96:
(7*2)+(6*4)+(5*5)+(4*6)+(3*2)+(2*9)+(1*6)=117
117 % 10 = 7
So 24562-96-7 is a valid CAS Registry Number.
24562-96-7Relevant academic research and scientific papers
REDUCTION OF C-0 BONDS BY CATALYTIC TRANSFER HYDROGENOLYSIS
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Page/Page column 15-16, (2012/09/22)
The present invention relates to a method of reducing a C-O bond to the corresponding C-H bond in a substrate which could be a benzylic alcohol, allylic alcohol, ester,or ether or an ether bond beta to a hydroxyl group or alpha to a carbonyl group.
Synthesis and bioactivity of erythro-nordihydroguaiaretic acid, threo-(-)-saururenin and their analogues
Xia, Yamu,Zhang, Yuanyuan,Wang, Wei,Ding, Yining,He, Rui
experimental part, p. 1325 - 1335 (2011/09/12)
Full details of the total syntheses of erythro-nordihydroguaiaretic acid, threo-(-)-saururenin and their analogues are presented. The syntheses were based on a unified synthetic strategy involving the Stobbe reaction, alkylation to construct the skeleton
Synthesis, anti-virus and anti-tumour activities of dibenzylbutyrolactone lignans and their analogues
Xia, Yamu,You, Jia,Zhang, Yuanyuan,Su, Zhongliang
experimental part, p. 565 - 569 (2010/03/03)
An efficient synthesis of dibenzylbutyrolactone lignans and their analogues has been developed. Based on a Stobbe condensation of piperonal or veratraldehyde with diethylsuccinate and alkylation with 3,4- methylenedioxybenzyl bromide to give the skeleton
