39251-40-6 Usage
Description
(R)-AMINO-PHENYL-ACETIC ACID ETHYL ESTER, with the molecular formula C10H13NO2, is an ethyl ester derivative of amino-phenyl-acetic acid. This chemical compound is widely utilized in the synthesis of pharmaceutical and agrochemical compounds. As a chiral compound, it possesses two enantiomers with distinct optical properties, making it a valuable building block for the development of various biologically active compounds. Its potential for diverse applications in organic chemistry positions it as a promising substance in the creation of new drugs and insecticides.
Uses
Used in Pharmaceutical Industry:
(R)-AMINO-PHENYL-ACETIC ACID ETHYL ESTER is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its role in the development of new drugs is attributed to its ability to serve as a versatile building block, allowing for the creation of a wide range of biologically active molecules.
Used in Agrochemical Industry:
In the agrochemical industry, (R)-AMINO-PHENYL-ACETIC ACID ETHYL ESTER is employed as a crucial component in the synthesis of insecticides. Its incorporation into these products enhances their effectiveness in controlling and managing pest populations, contributing to improved agricultural yields and crop protection.
Used in Organic Chemistry Research:
(R)-AMINO-PHENYL-ACETIC ACID ETHYL ESTER is also utilized as a valuable research tool in the field of organic chemistry. Its unique properties as a chiral compound make it an attractive candidate for studying the effects of stereochemistry on the biological activity of synthesized compounds, furthering our understanding of molecular interactions and the development of more effective drugs and chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 39251-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,5 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39251-40:
(7*3)+(6*9)+(5*2)+(4*5)+(3*1)+(2*4)+(1*0)=116
116 % 10 = 6
So 39251-40-6 is a valid CAS Registry Number.
39251-40-6Relevant articles and documents
Stereospecific Synthesis of 3,4-Dihydro-2 H-naphtho-1,4-oxazin-2-ones by Unification of Benzoxepine-4-carboxylates with Chiral Amino Acid Ethyl Esters
Bhimapaka, China Raju,Kasagani, Veera Prasad,Kurma, Siva Hariprasad
supporting information, p. 2976 - 2983 (2020/03/23)
A novel and efficient stereocontrolled method has been developed for the preparation of chiral 3,4-dihydro-2H-naphtho[1,2-b][1,4]oxazin-2-ones by the reaction of benzoxepine-4-carboxylates with chiral amino acid ethyl esters for the first time. The chiral 3,4-dihydro-2H-naphtho-1,4-oxazinones have been achieved in one step by the formation of C-N, C-C, and C-O bonds.
Boron-Catalyzed Azide Insertion of α-Aryl α-Diazoesters
San, Htet Htet,Wang, Chun-Ying,Zeng, Hai-Peng,Fu, Shi-Tao,Tang, Xiang-Ying,Jiang, Min
, p. 4478 - 4485 (2019/05/01)
A challenging metal-free azide insertion of α-aryl α-diazoesters in the presence of B(C6F5)3 (5 mol %) was developed for the first time. The reaction features an easy operation, wide substrate scope, and mild conditions an
Site-Selective γ-C(sp3)?H and γ-C(sp2)?H Arylation of Free Amino Esters Promoted by a Catalytic Transient Directing Group
Lin, Hua,Wang, Chao,Bannister, Thomas D.,Kamenecka, Theodore M.
supporting information, p. 9535 - 9541 (2018/07/14)
The first selective PdII-catalysed γ-C(sp3)?H and γ-C(sp2)?H arylation of free amino esters using a commercially available catalytic transient directing group. A variety of free amino esters, including α-amino esters and β-amino esters, amino monoesters and amino bis-esters, are shown to react with a diverse range of simple aryl and heteroaryl iodide reagents.
