1166394-91-7 Usage
Description
(R)-tert-butyl 4-(4-hydroxybutyl)-2,2-dimethyloxazolidine-3-carboxylate is a chemical compound that is a derivative of oxazolidine, a heterocyclic compound with nitrogen and oxygen atoms in its ring structure. (R)-tert-butyl 4-(4-hydroxybutyl)-2,2-diMethyloxazolidine-3-carboxylate features a tert-butyl group and a hydroxybutyl group attached to the oxazolidine ring, along with a carboxylate group. Its unique stereochemistry and structural features make it a promising candidate for drug design and synthesis in the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
(R)-tert-butyl 4-(4-hydroxybutyl)-2,2-dimethyloxazolidine-3-carboxylate is used as a potential building block for drug design and synthesis due to its versatile functional groups and unique stereochemistry. Its structural features make it valuable for the development of new pharmaceuticals targeting specific biological pathways.
Further research and testing are required to fully explore the potential of this compound in the medical field, as its specific applications and efficacy in drug development are yet to be determined.
Check Digit Verification of cas no
The CAS Registry Mumber 1166394-91-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,6,3,9 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1166394-91:
(9*1)+(8*1)+(7*6)+(6*6)+(5*3)+(4*9)+(3*4)+(2*9)+(1*1)=177
177 % 10 = 7
So 1166394-91-7 is a valid CAS Registry Number.
1166394-91-7Relevant articles and documents
Synthesis of 2-aminosuberic acid derivatives as components of some histone deacetylase inhibiting cyclic tetrapeptides
Chattopadhyay, Shital Kumar,Sil, Suman,Mukherjee, Jyoti Prasad
, p. 2153 - 2156 (2017)
A new synthesis of the important amino acid 2-aminosuberic acid from aspartic acid is reported. The methodology involves the alternate preparation of (S)-2-aminohept-6-enoate ester as a building block and its diversification through a cross-metathesis reaction to prepare the title compounds. The utility of the protocol is demonstrated through the preparation of three suberic acid derivatives of relevance to the design and the synthesis of peptides of biological relevance.
Stereoselective total synthesis of alkaloid caulophyllumine B using iterative olefin cross-metathesis protocol
Radha Krishna, Palakodety,Reddy, Bonepally Karunakar
scheme or table, p. 6262 - 6264 (2011/01/04)
Herein we report the first total synthesis of alkaloid caulophyllumine B in 14 steps by an iterative olefin cross-metathesis strategy from l-glutamic acid.
