1242267-80-6 Usage
General Description
(S)-Di-tert-butyl2-cyanopiperazine-1,4-dicarboxylate is a chemical compound that belongs to the family of piperazine derivatives. It is a white solid substance that is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. (S)-Di-tert-butyl2-cyanopiperazine-1,4-dicarboxylate is known for its versatile applications in the field of medicinal chemistry, particularly in the development of potential drug candidates. Its unique molecular structure and reactivity make it a valuable building block for the preparation of various biologically active molecules. Additionally, (S)-Di-tert-butyl2-cyanopiperazine-1,4-dicarboxylate is also used in organic synthesis and as a precursor in the manufacturing of specialty chemicals. Overall, it is an important compound with diverse industrial and scientific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1242267-80-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,2,6 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1242267-80:
(9*1)+(8*2)+(7*4)+(6*2)+(5*2)+(4*6)+(3*7)+(2*8)+(1*0)=136
136 % 10 = 6
So 1242267-80-6 is a valid CAS Registry Number.
1242267-80-6Relevant articles and documents
C(sp3)?H Cyanation Promoted by Visible-Light Photoredox/Phosphate Hybrid Catalysis
Wakaki, Takayuki,Sakai, Kentaro,Enomoto, Takafumi,Kondo, Mio,Masaoka, Shigeyuki,Oisaki, Kounosuke,Kanai, Motomu
, p. 8051 - 8055 (2018/06/15)
Inspired by the reaction mechanism of photo-induced DNA cleavage in nature, a C(sp3)?H cyanation reaction promoted by visible-light photoredox/phosphate hybrid catalysis was developed. Phosphate radicals, generated by one-electron photooxidation of phosphate salt, functioned as a hydrogen-atom-transfer catalyst to produce nucleophilic carbon radicals from C(sp3)?H bonds with a high bond-dissociation energy. The resulting carbon radicals were trapped by a cyano radical source (TsCN) to produce the C?H cyanation products. Due to the high functional-group tolerance and versatility of the cyano group, the reaction will be useful for realizing streamlined building block syntheses and late-stage functionalization of drug-like molecules.
