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Carbamic acid, (1,1-dimethylethyl)-, ethyl ester, also known as ethyl (1,1-dimethylethyl)carbamate, is an organic compound with the chemical formula C7H15NO2. It is a colorless liquid with a molecular weight of 145.2 g/mol. This ester is formed by the reaction of carbamic acid with ethyl alcohol and is a derivative of carbamic acid, where the hydrogen atom is replaced by an ethyl group. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is important to handle Carbamic acid, (1,1-dimethylethyl)-, ethyl ester with care, as it can be toxic and harmful if inhaled or ingested.

1611-50-3

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1611-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1611-50-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1611-50:
(6*1)+(5*6)+(4*1)+(3*1)+(2*5)+(1*0)=53
53 % 10 = 3
So 1611-50-3 is a valid CAS Registry Number.

1611-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-tert-butylcarbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,(1,1-dimethylethyl)-,ethyl 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:1611-50-3 SDS

1611-50-3Relevant academic research and scientific papers

New reactivity of oxaziridine: Pd(II)-catalyzed aromatic C-H ethoxycarbonylation via C-C bond cleavage

Peng, Xingao,Zhu, Yingguang,Ramirez, Thomas A.,Zhao, Baoguo,Shi, Yian

supporting information; experimental part, p. 5244 - 5247 (2011/12/04)

A novel Pd(II)-catalyzed aromatic C-H ethoxycarbonylation with oxaziridine involving C-C bond cleavage is described. Various aromatic 2-phenylpyridines and related compounds as well as aryl ureas can be effectively ethoxycarbonylated. A catalytic cycle in

Substituted N-phenyl 2-hydroxy-2-methyl-3,3,3-trifluoropropanamide derivatives which elevate pyruvate dehydrogenase activity

-

Page column 48, (2010/02/05)

A compound of formula (I) wherein: n is 1 or 2; R 1 is chloro, fluoro, bromo, methyl or methoxy; R 2 is as defined within; R 3 is as defined within; and R 4 is hydrogen or fluoro; or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof is described. The use of compounds of formula (I) in the production of an elevation of PDH activity in a warm-blooded animal such as a human being are also described. Pharmaceutical compositions, methods and processes for preparation of compounds of formula (I) are detailed. STR1

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