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910308-92-8

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  • Carbamic acid, [(1S)-1-(3-bromophenyl)-2-hydroxyethyl]-, 1,1-dimethylethyl ester (9CI)

    Cas No: 910308-92-8

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910308-92-8 Usage

General Description

(S)-b-(Boc-aMino)-3-broMobenzeneethanol is a chemical compound that belongs to the family of amino alcohols. It is a chiral compound with a specific orientation in space, denoted by the (S) in its name. The compound contains a tert-butyloxycarbonyl (Boc) protected amino group, a bromine atom, and an ethyl group attached to a benzene ring. (S)-b-(Boc-aMino)-3-broMobenzeneethanol has potential applications in organic synthesis, pharmaceuticals, and materials science due to its unique structure and reactivity. It can be used as a building block for the preparation of various biologically active compounds and can also serve as a valuable intermediate in the production of complex molecules. Overall, (S)-b-(Boc-aMino)-3-broMobenzeneethanol is a versatile compound with potential for a wide range of chemical and biomedical 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.

910308-92-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl [(1S)-1-(3-bromophenyl)-2-hydroxyethyl]carbam ate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:910308-92-8 SDS

910308-92-8Downstream Products

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.

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