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Ethyl 3,3,3-trifluoro-2-{[(4-methylphenyl)carbamoyl]amino}-2-phenylpropanoate is a complex organic compound with the molecular formula C20H20F3N2O4. It is a derivative of a carboxylic acid ester, specifically an ethyl ester, and features a trifluoromethyl group, a 4-methylphenyl group, and a carbamoyl group. ethyl 3,3,3-trifluoro-2-{[(4-methylphenyl)carbamoyl]amino}-2-phenylpropanoate is characterized by its unique structure, which includes a 2-phenylpropanoate backbone with a carbamoyl-linked 4-methylphenyl group and a trifluoroethyl moiety. It is likely to be found in pharmaceutical or chemical research settings, potentially as an intermediate in the synthesis of more complex molecules or as a compound with specific properties under investigation. Due to its intricate structure, it may have applications in the development of new drugs or materials, although its specific uses and properties would require further study and characterization.

6334-21-0

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6334-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6334-21-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6334-21:
(6*6)+(5*3)+(4*3)+(3*4)+(2*2)+(1*1)=80
80 % 10 = 0
So 6334-21-0 is a valid CAS Registry Number.

6334-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Benzolsulfonylamino-2-methyl-phenol

1.2 Other means of identification

Product number -
Other names 2-iodo-N-phenylsulfonyl-indole

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:6334-21-0 SDS

6334-21-0Relevant academic research and scientific papers

Reaction of N-sulfonyl derivatives of 1,4-benzoquinone monoimine with substituted hydrazines

Konovalova,Avdeenko,Goncharova,D’yakonenko,Shishkina

, p. 644 - 649 (2016/07/06)

Reaction direction of N-sulfonyl derivatives of 1,4-benzoquinone monoimine with substituted hydrazines depends on the redox potential of the quinone imine and on the basicity of the hydrazine. Aryl (alkyl)hydrazines of high basicity favor the reduction of

Synthesis of 5-substituted 2,3-dihydrobenzofurans in a one-pot oxidation/cyclization reaction

Baragona, Fabien,Lomberget, Thierry,Duchamp, Christian,Henriques, Natali,Lo Piccolo, Eugenio,Diana, Patrizia,Montalbano, Alessandra,Barret, Roland

experimental part, p. 8731 - 8739 (2011/12/02)

Variously substituted 2,3-dihydrobenzofurans have been synthesized according to a sequential one-pot oxidation/cyclization procedure between para-aminophenol derivatives and an azadiene.

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