136315-71-4 Usage
General Description
Boc-trans-2-amino cyclopentane carboxylic acid is a chemical compound that consists of a cyclopentane ring with an amino group and a carboxylic acid group attached to it. The abbreviation "Boc" stands for tert-butoxycarbonyl, which is a protecting group used in organic synthesis to protect the amino group from unwanted reactions. Boc-trans-2-aMinocyclopentane
carboxylic acid is an important intermediate in the synthesis of various pharmaceuticals and biologically active molecules. It is commonly used in peptide synthesis and as a building block in organic chemistry. Its unique structure and reactivity make it a versatile and valuable compound in the field of organic chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 136315-71-4 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 136315-71:
(8*1)+(7*3)+(6*6)+(5*3)+(4*1)+(3*5)+(2*7)+(1*1)=114
114 % 10 = 4
So 136315-71-4 is a valid CAS Registry Number.
136315-71-4Relevant articles and documents
Radical cyclization in heterocycle synthesis. Part 13: Sulfanyl radical addition-cyclization of oxime ethers and hydrazones connected with alkenes for synthesis of cyclic β-amino acids
Miyata, Okiko,Muroya, Kanami,Kobayashi, Tomoko,Yamanaka, Rina,Kajisa, Seiko,Koide, Junko,Naito, Takeaki
, p. 4459 - 4479 (2007/10/03)
A combination of sulfanyl radical addition-cyclization of the oxime ethers and hydrazones connected with alkenes and subsequent conversion of a phenylsulfanylmethyl group to a carboxyl group provides a novel method for the construction of the cyclic β-amino acids. Upon treatment with thiophenol in the presence of AIBN, the oxime ethers and hydrazones smoothly underwent sulfanyl radical addition-cyclization to give the 2-(phenylsulfanylmethyl)cycloalkylamine. This method was successfully applied to the practical synthesis of 2-aminocyclopentanecarboxylic acid and 4-amino-3-pyrrolidinecarboxylic acid.