905991-90-4 Usage
Description
METHYL (3R)-3-AMINO-3-(3-CHLOROPHENYL)PROPANOATE is a chemical compound with the formula C11H14ClNO2. It is a derivative of the amino acid phenylalanine, containing a methyl ester group, an amino group, and a chlorophenyl group. METHYL (3R)-3-AMINO-3-(3-CHLOROPHENYL)PROPANOATE is commonly used in the synthesis of pharmaceuticals and agrochemicals, and it has been studied for its potential therapeutic applications in the treatment of neurological disorders and as a building block for the creation of new drug molecules. It is important to handle this compound with care due to its potential for toxic effects if not used properly.
Uses
Used in Pharmaceutical Industry:
METHYL (3R)-3-AMINO-3-(3-CHLOROPHENYL)PROPANOATE is used as an intermediate in the synthesis of pharmaceuticals for its potential therapeutic applications in the treatment of neurological disorders.
Used in Agrochemical Industry:
METHYL (3R)-3-AMINO-3-(3-CHLOROPHENYL)PROPANOATE is used as a building block in the creation of new agrochemical molecules for pest control and crop protection.
Used in Drug Development:
METHYL (3R)-3-AMINO-3-(3-CHLOROPHENYL)PROPANOATE is used as a research compound for the development of new drug molecules, given its potential therapeutic properties and structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 905991-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,9,9 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 905991-90:
(8*9)+(7*0)+(6*5)+(5*9)+(4*9)+(3*1)+(2*9)+(1*0)=204
204 % 10 = 4
So 905991-90-4 is a valid CAS Registry Number.
905991-90-4Relevant articles and documents
Synthesis, in vitro and in vivo biological evaluation, and comprehensive understanding of structure-activity relationships of dipeptidyl boronic acid proteasome inhibitors constructed from β-amino acids
Zhu, Yongqiang,Wu, Gang,Zhu, Xinrong,Ma, Yuheng,Zhao, Xin,Li, Yuejie,Yuan, Yunxia,Yang, Jie,Yu, Sen,Shao, Feng,Lei, Meng
supporting information; experimental part, p. 8619 - 8626 (2011/03/20)
An extensive structure-activity relationship (SAR) study of 72 dipeptidyl boronic acid proteasome inhibitors constructed fromβ -amino acids is reported. SAR analysis revealed that bicyclic groups at the R1 position, 3-F substituents at the Rsu
ARYLAMIDES
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Page/Page column 48, (2010/02/06)
The invention relates to compounds of formula (I), to a method for their production, to pharmaceutical compositions containing said compounds and to their use for the treatment and/or prophylaxis of human or animal diseases, in particular bacterial infections.
The asymmetric synthesis of β-haloaryl-β-amino acid derivatives
Bull,Davies,Delgado-Ballester,Fenton,Kelly,Smith
, p. 1257 - 1260 (2007/10/03)
Lithium N-benzyl-N-α-methyl-4-methoxybenzylamide is employed as a homochiral ammonia equivalent for the asymmetric synthesis of β-haloaryl-β-amino acid derivatives using a conjugate addition/oxidative deprotection strategy.
