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Carbamic acid, (1-oxopropyl)-, 1,1-dimethylethyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120157-99-5

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120157-99-5 Usage

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 36, p. 3125, 1988 DOI: 10.1248/cpb.36.3125

Check Digit Verification of cas no

The CAS Registry Mumber 120157-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,5 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120157-99:
(8*1)+(7*2)+(6*0)+(5*1)+(4*5)+(3*7)+(2*9)+(1*9)=95
95 % 10 = 5
So 120157-99-5 is a valid CAS Registry Number.

120157-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-propanoylcarbamate

1.2 Other means of identification

Product number -
Other names N-propanoyl-carbamic acid tert-butyl ester

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:120157-99-5 SDS

120157-99-5Downstream Products

120157-99-5Relevant academic research and scientific papers

PURINE DERIVATIVES WITH ACTIVITY TO THE ADENOSINE A2A RECEPTOR

-

Page/Page column 43, (2008/06/13)

A compound of formula (I) or stereoisomers or pharmaceutically acceptable salts thereof, and their preparation and use as pharmaceuticals wherein U, R1, R2 and R3 are as defined herein.

PURINE DERIVATIVES FOR USE AS ADENOSIN A-2A RECEPTOR AGONISTS

-

Page/Page column 46, (2010/11/08)

Compounds of formula (I) in free or salt form, wherein R1, R2 and R3 have the meanings as indicated in the specification, are useful for treating conditions mediated by activation of the adenosine A2A receptor,

Synthesis of optically active β,γ-alkynylglycine derivatives

Meffre, Patrick,Gauzy, Laurence,Branquet, Eric,Durand, Philippe,Le Goffic, Francois

, p. 11215 - 11238 (2007/10/03)

Full results on the first synthesis of optically active β,γ-alkynylglycine derivatives from naturally occurring L-serine are described. The methodology uses L-serinal as a key intermediate and allows great versatility in the introduction of N-protective groups and of alkyne substitution. The N-Boc protected β,γ-alkynylglycine derivatives described have ee greater than 90%.

En route to optically active ethynylglycine derivatives

Meffre, Patrick,Gauzy, Laurence,Perdigues, Chantal,Desanges-Levecque, Florence,Branquet, Eric,Durand, Philippe,Le Goffic, Francois

, p. 877 - 880 (2007/10/02)

First results in the synthesis of chiral non racemic ethynylglycine derivatives from protected L-serinal are described.

A New Method for the Synthesis of Amides from Amines: Ruthenium Tetroxide Oxidation of N-Protected Alkylamines

Tanaka, Ken-Ichi,Yoshifuji, Shigeyuki,Nitta, Yoshihiro

, p. 3125 - 3129 (2007/10/02)

A simple synthetic method for the preparation of amides from the corresponding primary alkylamines was elaborated using ruthenium tetroxide (RuO4) oxidation as a key step.

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