115224-13-0 Usage
Description
(R)-A-PHENYL-3-BUTENAMINE, also known as (R)-1-amino-1-phenyl-3-buten-2-ol, is an organic compound with the chemical formula C10H13N. It belongs to the class of amines and is a chiral compound, existing in two enantiomeric forms, (R)and (S)-. (R)-A-PHENYL-3-BUTENAMINE is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, making it an important building block in the chemical and pharmaceutical industries.
Uses
Used in Pharmaceutical Industry:
(R)-A-PHENYL-3-BUTENAMINE is used as an intermediate for the synthesis of various drugs, including potential antitumor and antidepressant medications. Its chiral nature allows for the development of targeted therapies that can selectively interact with specific biological targets, improving the efficacy and safety of these medications.
Used in Agrochemical Industry:
(R)-A-PHENYL-3-BUTENAMINE is also used as an intermediate in the synthesis of agrochemicals, contributing to the development of more effective and selective pesticides and other agricultural products.
Used in Organic Chemistry:
(R)-A-PHENYL-3-BUTENAMINE serves as a key building block in the synthesis of chiral ligands and catalysts for asymmetric transformations in organic chemistry. These chiral catalysts and ligands are essential for the production of enantiomerically pure compounds, which are crucial in various applications, including pharmaceuticals, fragrances, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 115224-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,2 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115224-13:
(8*1)+(7*1)+(6*5)+(5*2)+(4*2)+(3*4)+(2*1)+(1*3)=80
80 % 10 = 0
So 115224-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H13N/c1-2-6-10(11)9-7-4-3-5-8-9/h2-5,7-8,10H,1,6,11H2/t10-/m1/s1
115224-13-0Relevant articles and documents
Synthesis and catalytic application of chiral 1,1′-bi-2-naphthol-and biphenanthrol-based pincer complexes: Selective allylation of sulfonimines with allyl stannane and allyl trifluoroborate
Aydin, Juhanes,Kumar, K. Senthil,Sayah, Mahmoud J.,Wallner, Olov A.,Szabo, Kalman J.
, p. 4689 - 4697 (2007)
(Chemical Equation Presented) New easily accessible 1,1′-bi-2- naphthol- (BINOL-) and biphenanthrol-based chiral pincer complex catalysts were prepared for selective (up to 85% enantiomeric excess) allylation of sulfonimines. The chiral pincer complexes w
Enantioselective Strecker and Allylation Reactions with Aldimines Catalyzed by Chiral Oxazaborolidinium Ions
Kang, Ki-Tae,Park, Sang Hyun,Ryu, Do Hyun
, p. 6679 - 6683 (2019/09/12)
Chiral oxazaborolidinium ion (COBI)-catalyzed enantioselective nucleophilic addition reactions of aldimines using tributyltin cyanide and allyltributylstannane have been developed. Various α-aminonitriles and homoallylic amines were synthesized in high yi
Copper-catalyzed asymmetric allylation of chiral N-tert-butanesulfinyl imines: Dual stereocontrol with nearly perfect diastereoselectivity
Zhao, Yi-Shuang,Liu, Qiang,Tian, Ping,Tao, Jing-Chao,Lin, Guo-Qiang
supporting information, p. 4174 - 4178 (2015/04/14)
Copper-catalyzed asymmetric allylation of chiral N-tert-butanesulfinyl imines has been described. Dual stereocontrol, through the combination of a chiral auxiliary and a chiral copper complex, has played an important role in achieving the nearly perfect d
