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6307-10-4

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6307-10-4 Usage

Aromatic carboxylic acid

The compound belongs to the class of aromatic carboxylic acids, which are characterized by the presence of a carboxyl group (-COOH) attached to an aromatic ring, such as a benzene ring.

Nitro group

The compound contains a nitro group (-NO2) attached to a phenyl ring. A nitro group is a functional group consisting of an oxygen-nitrogen-oxygen bond (-O-N=O), which is known for its strong electron-withdrawing properties.

Carbamoyl group

2-[(4-nitrophenyl)carbamoyl]benzoic acid also contains a carbamoyl group (-NH2CO-) attached to a benzene ring. A carbamoyl group is a functional group consisting of an amide bond (-NH2) and a carbonyl group (-CO-), which can participate in various chemical reactions.

Building block in organic synthesis

The compound is commonly used in organic synthesis and research as a building block for creating various pharmaceuticals and other organic compounds. This means that it can be used as a starting material or intermediate in the synthesis of more complex molecules.

Valuable tool in chemistry and pharmaceutical research

The unique structure and properties of 2-[(4-nitrophenyl)carbamoyl]benzoic acid make it a valuable tool for the development of new materials and chemical compounds. This implies that it can be used to create novel compounds with potential applications in various fields, such as medicine, materials science, and more.

Check Digit Verification of cas no

The CAS Registry Mumber 6307-10-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6307-10:
(6*6)+(5*3)+(4*0)+(3*7)+(2*1)+(1*0)=74
74 % 10 = 4
So 6307-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O5/c17-13(11-3-1-2-4-12(11)14(18)19)15-9-5-7-10(8-6-9)16(20)21/h1-8H,(H,15,17)(H,18,19)

6307-10-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-nitrophenyl)carbamoyl]benzoic acid

1.2 Other means of identification

Product number -
Other names Phthalanilic acid,4'-nitro

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:6307-10-4 SDS

6307-10-4Relevant articles and documents

Compounds and methods for inducing chondrogenesis

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Page/Page column 38; 101; 102, (2016/10/31)

The present invention provides compounds and compositions for the amelioration of arthritis and joint injuries by inducing mesenchymal stem cells into chondrocytes.

Solvent-mediated one-pot synthesis of cyclic N-Substituted imides

Patil, Sambhaji V.,Mahale, Keshao A.,Gosavi, Kirankumar S.,Deshmukh, Ganesh B.,Patil, Nilesh S.

, p. 314 - 320 (2013/07/26)

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Synthesis, characterization and biological studies of 2-(4- Nitrophenylamino-carbonyl)benzoic acid and its complexes with Cr(III), Co(II), Ni(II), Cu(II) and Zn(II)

Imran, Muhammad,Nazir, Sumaira,Latif, Shoomaila,Mahmood, Zaid

experimental part, p. 492 - 496 (2010/11/17)

Cr(III), Co(II), Ni(II), Cu(II) and Zn(II) complexes of 2-(4-Nitrophenylaminocarbonyl)benzoic acid were synthesized and characterized on the basis of physical, analytical and spectroscopic data. The ligands, as well as its metal complexes were checked for their in-vitro antimicrobial activity against three bacterial strains, Mycobacterium smegmatis, Escherichia coli, Pseudomonas aeuroginosa, and three fungal strains, Nigrospora oryzae, Aspergillus niger and Candida albicans. Disc diffusion method and Tube diffusion test were used for antibacterial and antifungal activities, respectively. The synthesized complexes only show significant antifungal activity but inactive for antibacterial, however, in general, the metal complexes were found to be more active against antimicrobial activities as compared to their uncomplexed ligand.

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