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Methyl N-(2,6-dimethylphenyl)-N-{[4-(phenylcarbonyl)phenyl]carbonyl}alaninate is a complex organic compound with the chemical formula C24H21NO4. It is a derivative of alanine, an amino acid, with two phenyl groups and a carbonyl group attached to the nitrogen atom. The compound features a methyl group at the alanine nitrogen, a 2,6-dimethylphenyl group, and a 4-(phenylcarbonyl)phenyl group connected through a carbonyl bridge. This molecule is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a precursor in the synthesis of various biologically active compounds. Its structure and properties make it a versatile building block in the development of new drugs and chemical products.

5312-75-4

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5312-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5312-75-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5312-75:
(6*5)+(5*3)+(4*1)+(3*2)+(2*7)+(1*5)=74
74 % 10 = 4
So 5312-75-4 is a valid CAS Registry Number.

5312-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(N-(4-benzoylbenzoyl)-2,6-dimethylanilino)propanoate

1.2 Other means of identification

Product number -
Other names METHYL 2-[(4-BENZOYLBENZOYL)-(2,6-DIMETHYLPHENYL)AMINO]PROPANOATE

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:5312-75-4 SDS

5312-75-4Relevant academic research and scientific papers

Preparation method of 2,5-dichloro-4-aminobenzenesulfonyl fluoride

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Paragraph 0024-0035, (2020/11/09)

The invention discloses a preparation method of 2,5-dichloro-4-aminobenzenesulfonyl fluoride. The preparation method comprises the following steps: taking 2,5-dichloro-4-aminobenzenesulfonyl chlorideas an initial raw material, potassium hydrogen fluoride

Monoazo dyes which are free from water-solubilizing groups and which contain a fluorosulphonyl group and process for colouring polyamides and polyester materials therewith

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, (2008/06/13)

A process for coloring a synthetic textile material or fibre blend thereof which comprises applying to the synthetic textile material a compound or mixture thereof, which is free from water solubilizing groups, of Formula (1): wherein A and D each independently is an optionally substituted heterocyclic or carbocyclic group and at least one of A or D carries directly at least one --SO2 F group or carries a substituent to which at least one --SO2 F group is attached except for 4-(4-fluorosulphonylphenylazo)-N,N-dimethylaniline, provided that one of A or D is not 3,5-difluorosulphonylthien-2-yl, optionally substituted 1-phenyl-pyrazol-4-yl-5-one or STR1 or that one of A or D does not carry an --NCH2 CH(OH)CH2 Cl, --NCOCH2 Cl or --NCH2 CH2 SO2 F substituent. The presence of one or more --SO2 F groups in a dye molecule generally improves the properties of that dye and confers surprisingly good wet fastness and light fastness properties.

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