1001179-33-4 Usage
Description
(S)-3-((tert-butoxycarbonyl)(isopropyl)amino)-2-(4-chlorophenyl)propionic acid is a chiral molecule with an S configuration, consisting of a 4-chlorophenyl group, an isopropylamino group, and a propionic acid group. It also features a tert-butoxycarbonyl protective group, which is commonly used in organic chemistry as a building block for the synthesis of various pharmaceuticals, agrochemicals, and other biologically active compounds. This chemical has potential applications in the development of new drugs and treatments.
Uses
Used in Pharmaceutical Industry:
(S)-3-((tert-butoxycarbonyl)(isopropyl)amino)-2-(4-chlorophenyl)propionic acid is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and functional groups. Its chiral nature and the presence of different groups make it a versatile compound for creating new drugs and treatments.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-3-((tert-butoxycarbonyl)(isopropyl)amino)-2-(4-chlorophenyl)propionic acid is used as a starting material for the development of new agrochemicals. Its structural diversity allows for the creation of compounds with specific biological activities, such as pesticides or herbicides, that can be tailored to target specific pests or weeds.
Used in Research and Development:
(S)-3-((tert-butoxycarbonyl)(isopropyl)amino)-2-(4-chlorophenyl)propionic acid is also used in research and development for the creation of new biologically active compounds. Its unique structure and functional groups make it an attractive candidate for exploring novel chemical reactions and synthesizing new molecules with potential applications in various fields, including medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 1001179-33-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,1,7 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1001179-33:
(9*1)+(8*0)+(7*0)+(6*1)+(5*1)+(4*7)+(3*9)+(2*3)+(1*3)=84
84 % 10 = 4
So 1001179-33-4 is a valid CAS Registry Number.
1001179-33-4Relevant articles and documents
Asymmetric Synthesis of Akt Kinase Inhibitor Ipatasertib
Han, Chong,Savage, Scott,Al-Sayah, Mohammad,Yajima, Herbert,Remarchuk, Travis,Reents, Reinhard,Wirz, Beat,Iding, Hans,Bachmann, Stephan,Fantasia, Serena M.,Scalone, Michelangelo,Hell, André,Hidber, Pirmin,Gosselin, Francis
, p. 4806 - 4809 (2017/09/23)
A highly efficient asymmetric synthesis of the Akt kinase inhibitor ipatasertib (1) is reported. The bicyclic pyrimidine 2 starting material was prepared via a nitrilase biocatalytic resolution, halogen-metal exchange/anionic cyclization, and a highly dia
Synthesis of Akt inhibitor ipatasertib. part 2. Total synthesis and first kilogram scale-up
Remarchuk, Travis,St-Jean, Frederic,Carrera, Diane,Savage, Scott,Yajima, Herbert,Wong, Brian,Babu, Srinivasan,Deese, Alan,Stults, Jeffrey,Dong, Michael W.,Askin, David,Lane, Jonathan W.,Spencer, Keith L.
, p. 1652 - 1666 (2015/02/19)
Herein, the first-generation process to manufacture Akt inhibitor Ipatasertib through a late-stage convergent coupling of two challenging chiral components on multikilogram scale is described. The first of the two key components is a trans-substituted cyc
PROCESS FOR MAKING AMINO ACID COMPOUNDS
-
, (2013/12/03)
The invention provides new processes for making and purifying amino acid compounds, which are useful in the preparation of AKT inhibitors used in the treatment of diseases such as cancer, including the compound (S)-2-(4-chlorophenyl)-1-(4-((5R,7R)-7-hydroxy-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)piperazin-1-yl)-3-(isopropylamino)propan-1-one.
