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2-Fluoro-N-(4-Methylphenyl)benzamide, 97%, is a high-purity organic compound with the chemical formula C14H12FNO. It is a derivative of benzamide, featuring a fluorine atom at the 2nd position and a 4-methylphenyl group attached to the nitrogen atom. 2-Fluoro-N-(4-Methylphenyl)benzaMide, 97% is widely used in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. The 97% purity indicates that the product contains a minimum of 97% of the desired compound, with the remaining 3% being other substances, which could be impurities or by-products from the synthesis process.

6876-61-5

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6876-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6876-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,7 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6876-61:
(6*6)+(5*8)+(4*7)+(3*6)+(2*6)+(1*1)=135
135 % 10 = 5
So 6876-61-5 is a valid CAS Registry Number.

6876-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-N-(p-tolyl)benzamide

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

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

More Details:6876-61-5 SDS

6876-61-5Relevant academic research and scientific papers

Copper-catalyzed Goldberg-type C-N coupling in deep eutectic solvents (DESs) and water under aerobic conditions

Cicco, Luciana,Hernández-Fernández, Jose A.,Salomone, Antonio,Vitale, Paola,Ramos-Martín, Marina,González-Sabín, Javier,Presa Soto, Alejandro,Perna, Filippo M.,Capriati, Vito,García-álvarez, Joaquín

supporting information, p. 1773 - 1779 (2021/03/14)

An efficient and selectiveN-functionalization of amides is first reportedviaa CuI-catalyzed Goldberg-type C-N coupling reaction between aryl iodides and primary/secondary amides run either in Deep Eutectic Solvents (DESs) or water as sustainable reaction media, under mild and bench-type reaction conditions (absence of protecting atmosphere). Higher activities were observed in an aqueous medium, though the employment of DESs expanded and improved the scope of the reaction to include also aliphatic amides. Additional valuable features of the reported protocol include: (i) the possibility to scale up the reaction without any erosion of the yield/reaction time; (ii) the recyclability of both the catalyst and the eutectic solvent up to 4 consecutive runs; and (iii) the feasibility of the proposed catalytic system for the synthesis of biologically active molecules.

Amide Boc de-protection method

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Paragraph 0037; 0149; 0150; 0151, (2018/09/13)

The invention discloses an amide Boc de-protection method. The amide Boc de-protection method includes carrying out reaction on Boc protected amide III and amine IV under the condition of the presenceof palladium catalysts to generate new amide V. 8-aminoquinoline can be used as a guide group to be applied to chemical reaction, a process for synthesizing the new amide by means of de-protection isprovided, protecting groups can be easily removed by means of palladium catalysis, the new amide can be generated, and the reaction is high in efficiency. The amide Boc de-protection method has the advantages of environmental friendliness, recyclability and the like.

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