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3085-53-8

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3085-53-8 Usage

General Description

3-Methylformanilide is an organic chemical compound classified under the anilides group. It appears as a yellowish to colorless oily liquid and is known for its sweet, floral, and herbaceous odor. Its chemical formula is C9H11NO and its molecular weight is 149.19 g/mol. It is primarily used in blossoms for spicy, sweet, floral, and tobacco-like odor effects and is also used as a flavoring substance. Since it's moderately toxic, exposure to 3-Methylformanilide should be minimized. Its physical and chemical properties are fairly stable, making it suitable for various uses. Its use should be in compliance with FDA regulations regarding flavoring substances.

Check Digit Verification of cas no

The CAS Registry Mumber 3085-53-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3085-53:
(6*3)+(5*0)+(4*8)+(3*5)+(2*5)+(1*3)=78
78 % 10 = 8
So 3085-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO/c1-7-3-2-4-8(5-7)9-6-10/h2-6H,1H3,(H,9,10)

3085-53-8 Well-known Company Product Price

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  • Alfa Aesar

  • (B24061)  3-Methylformanilide, 97%   

  • 3085-53-8

  • 5g

  • 412.0CNY

  • Detail
  • Alfa Aesar

  • (B24061)  3-Methylformanilide, 97%   

  • 3085-53-8

  • 25g

  • 1752.0CNY

  • Detail
  • Alfa Aesar

  • (B24061)  3-Methylformanilide, 97%   

  • 3085-53-8

  • 100g

  • 6323.0CNY

  • Detail

3085-53-8SDS

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 N-(3-methylphenyl)formamide

1.2 Other means of identification

Product number -
Other names Formamide, N-(3-methylphenyl)-

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:3085-53-8 SDS

3085-53-8Relevant articles and documents

Copper-Catalyzed Cascade N-Dealkylation/N-Methyl Oxidation of Aromatic Amines by Using TEMPO and Oxygen as Oxidants

Li, Dianjun,Wang, Shihaozhi,Yang, Jiale,Yang, Jinhui

supporting information, p. 6768 - 6772 (2021/12/31)

A novel tandem N-dealkylation and N-methyl aerobic oxidation of tertiary aromatic amines to N-arylformamides using copper and TEMPO has been developed. This methodology suggested an alternative synthetic route from N-methylarylamines to N-arylformamides.

An Environmentally Benign, Catalyst-Free N?C Bond Cleavage/Formation of Primary, Secondary, and Tertiary Unactivated Amides

Kumar, Vishal,Dhawan, Sanjeev,Girase, Pankaj Sanjay,Singh, Parvesh,Karpoormath, Rajshekhar

, p. 5627 - 5639 (2021/11/11)

Herein, we report an operationally simple, cheap, and catalyst-free method for the transamidation of a diverse range of unactivated amides furnishing the desired products in excellent yields. This protocol is environmentally friendly and operates under extremely mild conditions without using any promoter or additives. Significantly, this strategy has been implied in the chemoselective synthesis of a pharmaceutical molecule, paracetamol, on a gram-scale with excellent yield. We anticipate that this universally applicable strategy will be of great interest in drug discovery, biochemistry, and organic synthesis.

Palladium supported on MRGO@CoAl-LDH catalyzed reductive carbonylation of nitroarenes and carbonylative Suzuki coupling reactions using formic acid as liquid CO and H2 source

Jadidi Nejad, Masoumeh,Heydari, Akbar

, (2021/07/17)

In the present study, a heterogeneous palladium catalyst system, Pd nanoparticles supported on MRGO@CoAl-LDH, was synthesized and employed in reductive carbonylation of nitroarenes and carbonylative Suzuki coupling reactions using formic acid as CO and H2 source. The as-obtained heterogeneous catalyst was characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDAX), thermal gravimetric analysis (TGA), and vibrating sample magnetometer (VSM). The nanocatalyst was reused for 5 cycles with a negligible reduction in the yield of products. All reactions were carried out with high yields and under suitable and safe conditions. Also, we have successfully applied formic acid as a good and safe alternative to CO and H2 gases.

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