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N-(4-methoxy-2-methyl-phenyl)formamide is a formamide derivative with the molecular formula C9H11NO2. It features a formyl group attached to the nitrogen atom and a phenyl group attached to the carbon atom, with a methoxy and a methyl group on the phenyl ring, making it a substituted form of aniline.

7402-54-2

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7402-54-2 Usage

Uses

Used in Organic Synthesis:
N-(4-methoxy-2-methyl-phenyl)formamide is used as an intermediate in organic synthesis for the production of various drugs and pharmaceuticals.
Used in Pharmaceutical Research:
In pharmaceutical research, N-(4-methoxy-2-methyl-phenyl)formamide is used as a building block for the synthesis of novel pharmaceutical compounds.
Used in Medicinal Chemistry:
N-(4-methoxy-2-methyl-phenyl)formamide is important in medicinal chemistry due to its potential biological and pharmacological properties, such as antibacterial and anti-inflammatory effects.

Check Digit Verification of cas no

The CAS Registry Mumber 7402-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7402-54:
(6*7)+(5*4)+(4*0)+(3*2)+(2*5)+(1*4)=82
82 % 10 = 2
So 7402-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-7-5-8(12-2)3-4-9(7)10-6-11/h3-6H,1-2H3,(H,10,11)

7402-54-2SDS

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-(4-methoxy-2-methylphenyl)formamide

1.2 Other means of identification

Product number -
Other names 4-Methoxy-2-methyl-formanilid

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:7402-54-2 SDS

7402-54-2Relevant academic research and scientific papers

PYRIMIDINE COMPOUNDS AND PYRIMIDO INDOLE COMPOUNDS AND METHODS OF USE

-

Page/Page column 50, (2016/03/19)

The present invention discloses substituted pyrimidine and pyrimido indole compounds and optionally pharmaceutically acceptable salts, hydrates or solvates thereof. A method of treating a patient having cancer or a disease comprising administering to a patient an effective amount of the compound or pharmaceutically acceptable salt, hydrate, or solvate thereof.

Screw Sense Selective Polymerization of Achiral Isocyanides Catalysed by Optically Active Nickel(II) Complexes

Kamer, Paul C. J.,Nolte, Roeland J. M.,Drenth, Wiendelt

, p. 6818 - 6825 (2007/10/02)

Poly(isocyanides), (RN=Cn, can be prepared from isocyanides, , by the catalytic action of nickel(II) compounds.The main chain of these polymers is a rigid helix.This helical conformation results from a restricted rotation around the single bonds that connect the main-chain carbon atoms.Polymerization of achiral isocyanides generally gives a racemic mixture of left- and right-handed helices, whereas polymerization of optically active isocyanides results in helices with an excess of one screw sense.We describe a procedure for obtaining poly(isocyanides) with predominantly one screw sense, starting from an achiral monomer.A catalyst is prepared by adding an optically active amine to a tetrakis(isocyanide)nickel(II) perchlorate complex.Polymerization of various achiral isocyanides with this catalist yields optically active polymers with an enantiomeric excess up to 83percent.

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