136315-70-3 Usage
Description
CIS-2-(TERT-BUTOXYCARBONYLAMINO)-1-CYCLOPENTANECARBOXYLIC ACID, 98 is a carboxylic acid derivative characterized by its white to almost white fine crystalline powder appearance. It is a compound with pharmaceutical relevance due to its potential applications in the development of various drugs.
Uses
Used in Pharmaceutical Industry:
CIS-2-(TERT-BUTOXYCARBONYLAMINO)-1-CYCLOPENTANECARBOXYLIC ACID, 98 is used as a pharmaceutical intermediate for the synthesis of various drugs. Its carboxylic acid nature allows for the formation of esters, amides, and other derivatives, which can be further utilized in the development of therapeutic agents.
As a pharmaceutical intermediate, CIS-2-(TERT-BUTOXYCARBONYLAMINO)-1-CYCLOPENTANECARBOXYLIC ACID, 98 plays a crucial role in the synthesis of drugs targeting different medical conditions. Its versatility in chemical reactions enables the creation of a wide range of pharmaceutical compounds with diverse therapeutic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 136315-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136315-70:
(8*1)+(7*3)+(6*6)+(5*3)+(4*1)+(3*5)+(2*7)+(1*0)=113
113 % 10 = 3
So 136315-70-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NO4/c1-11(2,3)16-10(15)12-8-6-4-5-7(8)9(13)14/h7-8H,4-6H2,1-3H3,(H,12,15)(H,13,14)/t7-,8+/m1/s1
136315-70-3Relevant articles and documents
Amipurimycin: Total Synthesis of the Proposed Structures and Diastereoisomers
Wang, Shengyang,Sun, Jiansong,Zhang, Qingju,Cao, Xin,Zhao, Yachen,Tang, Gongli,Yu, Biao
supporting information, p. 2884 - 2888 (2018/02/16)
The proposed diastereoisomers (1 a–d) together with their C8′-epimers (1 e–h) of amipurimycin, a unique antifungal peptidyl nucleoside antibiotic, have been synthesized for the first time. The synthetic approach is efficient and stereodivergent, and features a stereoselective aldol condensation to build the branched C9 sugar amino acid skeleton and a regio- and stereocontrolled gold(I)-catalyzed N-glycosylation to furnish the purine nucleoside. Analysis of the NMR data suggests that the previously assigned configuration of the tertiary C3′ in amipurimycin should be of opposite configuration.
A concise synthesis of rigidified β-amino acids via sulfanyl radical addition-cyclization of oxime ethers and hydrazones
Miyata, Okiko,Muroya, Kanami,Koide, Junko,Naito, Takeaki
, p. 271 - 272 (2007/10/03)
A new route to the rigidified cyclic β-amino acids such as cispentacin has been developed by sulfanyl radical addition-cyclization of the alkenyl-tethered-oxime ethers and hydrazones.
