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[2-(4-HYDROXY-PHENYL)-2-OXO-ETHYL]-CARBAMIC ACID TERT-BUTYL ESTER is a chemical compound that is commonly used as a reagent in organic synthesis. It is a tert-butyl ester derivative of carbamic acid and contains a phenyl group with a hydroxyl and carbonyl group attached to the ethyl bridge. Its chemical structure and reactivity make it suitable for a wide range of applications in organic chemistry.
Used in Pharmaceutical Industry:
[2-(4-HYDROXY-PHENYL)-2-OXO-ETHYL]-CARBAMIC ACID TERT-BUTYL ESTER is used as a building block for the synthesis of other organic compounds, especially in the production of potential drug candidates.
Used in Chemical Industry:
[2-(4-HYDROXY-PHENYL)-2-OXO-ETHYL]-CARBAMIC ACID TERT-BUTYL ESTER is used as a reagent in organic synthesis for its chemical structure and reactivity.

607358-50-9

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607358-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 607358-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,3,5 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 607358-50:
(8*6)+(7*0)+(6*7)+(5*3)+(4*5)+(3*8)+(2*5)+(1*0)=159
159 % 10 = 9
So 607358-50-9 is a valid CAS Registry Number.

607358-50-9 Well-known Company Product Price

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  • Aldrich

  • (JWP00357)  [2-(4-Hydroxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester  AldrichCPR

  • 607358-50-9

  • JWP00357-1G

  • 5,476.77CNY

  • Detail

607358-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-{4-hydroxy-phenyl}-2-oxo-ethyl)-carbamic acid tert-butyl ester

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

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

More Details:607358-50-9 SDS

607358-50-9Relevant academic research and scientific papers

Fibrinogen receptor antagonists and their use

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Page/Page column 65, (2010/08/04)

This invention relates to novel fused bicyclic compounds of the general formula (I): wherein the symbols are defined herein, to pharmaceutical compositions containing the compounds, processes for preparing the compounds, and to methods of using the compounds, alone or in combination with other therapeutic agents. The compounds are antagonists of the platelet glycoprotein IIb/IIIa fibrinogen receptor complex, and are therefore useful for the inhibition of platelet aggregation, and for the treatment of thrombotic diseases and other diseases.

FIBRINOGEN RECEPTOR ANTAGONISTS AND THEIR USE

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Page/Page column 79, (2010/02/11)

This invention relates to novel fused bicyclic compounds of the general formula (I): wherein the symbols are defined herein, to pharmaceutical compositions containing the compounds, processes for preparing the compounds, and to methods of using the compounds, alone or in combination with other therapeutic agents. The compounds are antagonists of the platelet glycoprotein IIb/IIIa fibrinogen receptor complex, and are therefore useful for the inhibition of platelet aggregation, and for the treatment of thrombotic diseases and other diseases.

Synthesis of proposed oxidation-cyclization-methylation intermediates of the coumarin antibiotic biosynthetic pathway

Tao, Junhua,Hu, Shanghui,Pacholec, Michelle,Walsh, Christopher T.

, p. 3233 - 3236 (2007/10/03)

(Matrix presented) A chemoenzymatic synthesis was described to prepare proposed oxidation-cyclization-methylation intermediates of the coumarin antibiotic biosynthetic pathway. The successful synthesis of these fragile molecules relies heavily on mild enz

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