101382-85-8 Usage
Description
(2S,4R,6R)-7-(tert-Butyl-diphenyl-silanyloxy)-2,6-dimethyl-heptane-1,4-diol is a complex organic compound characterized by its unique structure and functional groups. It features a tert-butyl group, a diphenyl-silanyloxy group, and a diol moiety, along with two chiral centers that result in four possible stereoisomers. This long-chain hydrocarbon has a silanyloxy group attached to the seventh carbon and two hydroxyl groups on the first and fourth carbons, which may contribute to its potential applications in various fields such as pharmaceuticals and materials science.
Uses
Used in Pharmaceutical Industry:
(2S,4R,6R)-7-(tert-Butyl-diphenyl-silanyloxy)-2,6-dimethyl-heptane-1,4-diol is used as a potential pharmaceutical compound for its unique structure and functional groups. The presence of the diol moiety and hydroxyl groups may allow for the formation of hydrogen bonds, which can be crucial in drug design and interactions with biological targets.
Used in Materials Science:
In the field of materials science, (2S,4R,6R)-7-(tert-Butyl-diphenyl-silanyloxy)-2,6-dimethyl-heptane-1,4-diol may be utilized for its structural properties and the ability to form specific interactions due to its functional groups. (2S,4R,6R)-7-(tert-Butyl-diphenyl-silanyloxy)-2,6-dimethyl-heptane-1,4-diol's potential use in the development of new materials with tailored properties could be explored, such as in polymers, coatings, or adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 101382-85-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,3,8 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101382-85:
(8*1)+(7*0)+(6*1)+(5*3)+(4*8)+(3*2)+(2*8)+(1*5)=88
88 % 10 = 8
So 101382-85-8 is a valid CAS Registry Number.
101382-85-8Relevant articles and documents
A Tactically Novel Alternative to Acyclic Stereoselection Based on the Concept of a Replicating Chiron - 1,5-C-Methyl Substitution
Hanessian, Stephen,Murray, Peter J.,Sahoo, Soumya P.
, p. 5623 - 5626 (1985)
A synthetic sequence is described wherein a chiral butyrolactone is used as a template to control the stereochemistry of a C-methylation process on the corresponding enolate.A sequential two-carbon homologation and replication of the butyrolactone template allows a second stereocontrolled C-methylation.The ultimate outcome is a seven carbon acyclic chain with a predicable 1,5-substitution pattern of C-methyl groups with or without an intervening hydroxyl group.
