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"Acetamide, N-(4,5-dimethyl-2-nitrophenyl)-2,2,2-trifluoro-" is a complex organic chemical compound with the molecular formula C11H10F3N2O3. It is a derivative of acetamide, featuring a 4,5-dimethyl-2-nitrophenyl group attached to the nitrogen atom, and a trifluoroacetyl group. Acetamide, N-(4,5-dimethyl-2-nitrophenyl)-2,2,2-trifluoro- is characterized by its unique structure, which includes a nitro group, two methyl groups, and three fluorine atoms, contributing to its distinct chemical properties. It is typically synthesized for use in various chemical research applications, particularly in the field of pharmaceuticals and agrochemicals, where its specific functional groups may be exploited for the development of new compounds with potential biological activity.

1799-80-0

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1799-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1799-80-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1799-80:
(6*1)+(5*7)+(4*9)+(3*9)+(2*8)+(1*0)=120
120 % 10 = 0
So 1799-80-0 is a valid CAS Registry Number.

1799-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dimethyl-2-nitro-N-(trifluoroacetyl)aniline

1.2 Other means of identification

Product number -
Other names 4,5-Dimethyl-2-nitro-N-trifluoroacetylaniline

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:1799-80-0 SDS

1799-80-0Relevant articles and documents

Investigation of flavin-containing DNA-repair model compounds

Epple, Robert,Wallenborn, Ernst-Udo,Carell, Thomas

, p. 7440 - 7451 (2007/10/03)

Irradiation of DNA with UV-B light causes the formation of mutagenic DNA lesions such as cis-syn and trans-syn cyclobutane pyrimidine dimers. DNA photolyases are flavin-dependent repair enzymes which directly revert the mutagenic cis-syn pyrimidine dimers

Zur DNA-Reparatur durch das Enzym DNA-Photolyase: Synthese von Flavin enthaltenden Modellverbindungen

Carell, Thomas,Epple, Robert,Gramlich, Volker

, p. 676 - 679 (2007/10/03)

Keywords: DNA-Reparatur; Elektronentransfer; Flavine; Nucleobasen

A 'one-pot' phase transfer alkylation/hydrolysis of o-nitrotrifluoroacetanilides. A convenient route to N-alkyl o-phenylenediamines

Brown, Samuel A.,Rizzo, Carmelo J.

, p. 4065 - 4080 (2007/10/03)

A variety of o-nitrotrifluoroacetanilides undergo a one-pot alkylation/hydrolysis to give N-alkyl o-nitroanilines in 40-94% yield. Dimethylsulfate, benzyl bromide and 1-bromo-propane were used as the electrophiles.

?...? Interactions of Flavins, 5. Syntheses, Structures and Physical Properties of Flavin Systems with Covalent Bonding to ? Donors and ? Acceptors (Quinones)

Staab, Heinz A.,Kanellakopulos, Johannes,Kirsch, Peer,Krieger, Claus

, p. 1827 - 1836 (2007/10/03)

To study ?...? interactions of flavins of different redox states with ?-electron donorsand acceptors, the syntheses of compounds in which such ? systems are linked to flavins by using the "cyclophane concept" were attempted and partially achieved.The synt

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