910308-92-8 Usage
Description
(S)-b-(Boc-aMino)-3-broMobenzeneethanol is a chiral chemical compound belonging to the amino alcohols family. It features a specific spatial orientation, indicated by the (S) in its name, and consists of a tert-butyloxycarbonyl (Boc) protected amino group, a bromine atom, and an ethyl group attached to a benzene ring. This versatile compound holds potential applications in organic synthesis, pharmaceuticals, and materials science due to its unique structure and reactivity.
Uses
Used in Organic Synthesis:
(S)-b-(Boc-aMino)-3-broMobenzeneethanol is used as a building block for the preparation of various biologically active compounds, contributing to the development of new organic molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
(S)-b-(Boc-aMino)-3-broMobenzeneethanol is used as a valuable intermediate in the production of complex molecules, playing a crucial role in the synthesis of pharmaceutical compounds with potential therapeutic effects.
Used in Materials Science:
(S)-b-(Boc-aMino)-3-broMobenzeneethanol is used as a component in the development of novel materials, leveraging its unique structure and reactivity to create materials with enhanced properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 910308-92-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,3,0 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 910308-92:
(8*9)+(7*1)+(6*0)+(5*3)+(4*0)+(3*8)+(2*9)+(1*2)=138
138 % 10 = 8
So 910308-92-8 is a valid CAS Registry Number.
910308-92-8Relevant articles and documents
CTPS1 INHIBITORS AND USES THEREOF
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Paragraph 00965, (2022/05/02)
The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of CPTS1, and the treatment of CPTS1-mediated disorders.
Synthesis of enantiopure 1,2-azido and 1,2-amino alcohols via regio- and stereoselective ring-opening of enantiopure epoxides by sodium azide in hot water
Wang, Hai-Yang,Huang, Kun,De Jesús, Melvin,Espinosa, Sandraliz,Pi?ero-Santiago, Luis E.,Barnes, Charles L.,Ortiz-Marciales, Margarita
, p. 91 - 100 (2016/02/09)
A practical and convenient method for the efficient and regio- and stereoselective ring-opening of enantiopure monosubstituted epoxides by sodium azide under hydrolytic conditions is reported. The ring-opening of enantiopure styryl and pyridyl (S)-epoxides by N3- in hot water takes place preferentially at the internal position with complete inversion of configuration to produce (R)-2-azido ethanols with up to 99% enantio- and regioselectivity, while the (S)-adamantyl oxirane provides mainly the (S)-1-adamantyl-2-azido ethanol in excellent yield. In general, 1,2-amino ethanols were obtained in high yield and excellent enantiopurity by the reduction of the chiral 1,2-azido ethanols with PPh3 in water/THF, and then converted into the Boc or acetamide derivatives.