106910-76-3 Usage
Description
2-Benzylamino-3-hydroxypropionic Acid is a chemical compound that belongs to the class of organic compounds known as beta amino acids and derivatives. It is a derivative of phenylalanine, featuring a benzylamine group attached to the beta carbon of the amino acid. This unique structure and properties make it a promising candidate for various applications in the pharmaceutical industry, including drug development, medicinal chemistry, and the study of biochemical and metabolic pathways involving amino acids.
Uses
Used in Pharmaceutical Industry:
2-Benzylamino-3-hydroxypropionic Acid is used as a building block for drug development due to its unique structure and properties. It can be incorporated into the design of new pharmaceutical compounds, potentially leading to the discovery of novel therapeutic agents.
2-Benzylamino-3-hydroxypropionic Acid is used as a research tool in medicinal chemistry for studying the interactions of beta amino acids with biological targets and understanding their role in various biochemical and metabolic pathways.
Further research is needed to fully explore the potential uses and implications of 2-benzylamino-3-hydroxypropionic acid in the pharmaceutical industry and other related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 106910-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,1 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106910-76:
(8*1)+(7*0)+(6*6)+(5*9)+(4*1)+(3*0)+(2*7)+(1*6)=113
113 % 10 = 3
So 106910-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c12-7-9(10(13)14)11-6-8-4-2-1-3-5-8/h1-5,9,11-12H,6-7H2,(H,13,14)
106910-76-3Relevant articles and documents
A highly practical method for monobenzylation of amino acids
Shao, Hua-Wu,Wu, Yikang,Li, Rongxiu
, p. 1911 - 1915 (2000)
Amino acids are cleanly monobenzylated at ambient temperature using benzyl chloride in water containing potassium carbonate.
Selenoimidazolium Salts as Supramolecular Reagents for Protein Alkylation
Lim, David,Wen, Xiaojin,Seebeck, Florian P.
, p. 3515 - 3520 (2020/09/21)
Se-benzyl selenoimidazolium salts are characterized by remarkable alkyl-transfer potential under physiological conditions. Structure-activity relationship studies show that selective monoalkylation of primary amines depends on supramolecular interactions
Discovery and preclinical evaluation of [4-[[1-(3-fluorophenyl)methyl]-1H- indazol-5-ylamino]-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl]carbamic acid, (3S)-3-morpholinylmethyl ester (BMS-599626), a selective and orally efficacious inhibitor of human epide
Gavai, Ashvinikumar V.,Fink, Brian E.,Fairfax, David J.,Martin, Gregory S.,Rossiter, Lana M.,Holst, Christian L.,Kim, Soong-Hoon,Leavitt, Kenneth J.,Mastalerz, Harold,Han, Wen-Ching,Norris, Derek,Goyal, Bindu,Swaminathan, Shankar,Patel, Bharat,Mathur, Arvind,Vyas, Dolatrai M.,Tokarski, John S.,Chiang, Yu,Oppenheimer, Simone,Hongjian, Zhang,Marathe, Punit,Fargnoli, Joseph,Lee, Francis Y.,Wong, Tai W.,Vite, Gregory D.
supporting information; experimental part, p. 6527 - 6530 (2010/03/26)
Structure-activity relationships in a series of 4-[1H-indazol-5-ylamino] pyrrolo[2,1-f][1,2,4]triazine-6-carbamates identified dual human epidermal growth factor receptor (HER)1/HER2 kinase inhibitors with excellent biochemical potency and kinase selectiv