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2-(3-aminobenzoyl)benzoic acid is an organic compound with the molecular formula C14H11NO3. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. 2-(3-aminobenzoyl)benzoic acid is characterized by its two benzene rings, one of which is substituted with an amino group (-NH2) at the 3rd position, while the other is substituted with a carboxyl group (-COOH) at the 2nd position. The two benzene rings are connected through an amide linkage, forming a benzoyl group. 2-(3-aminobenzoyl)benzoic acid has potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity.

6268-18-4

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6268-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6268-18-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6268-18:
(6*6)+(5*2)+(4*6)+(3*8)+(2*1)+(1*8)=104
104 % 10 = 4
So 6268-18-4 is a valid CAS Registry Number.

6268-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-aminobenzoyl)benzoic acid

1.2 Other means of identification

Product number -
Other names HMS3080P03

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:6268-18-4 SDS

6268-18-4Relevant academic research and scientific papers

The discovery of 1,2,3,9b-tetrahydro-5H-imidazo[2,1-a]isoindol-5-ones as a new class of respiratory syncytial virus (RSV) fusion inhibitors. Part 1

Bond, Silas,Draffan, Alistair G.,Fenner, Jennifer E.,Lambert, John,Lim, Chin Yu,Lin, Bo,Luttick, Angela,Mitchell, Jeffrey P.,Morton, Craig J.,Nearn, Roland H.,Sanford, Vanessa,Stanislawski, Pauline C.,Tucker, Simon P.

, p. 969 - 975 (2015/02/19)

Respiratory syncytial virus (RSV) is a major cause of respiratory tract infections in infants, young children and adults. Compound 1a (9b-(4-chlorophenyl)-1-(4-fluorobenzoyl)-1,2,3,9b-tetrahydro-5H-imidazo[2,1-a]isoindol-5-one) was identified as an inhibitor of A and B strains of RSV targeting the fusion glycoprotein. SAR was developed by systematic exploration of the phenyl (R1) and benzoyl (R2) groups. Furthermore, introduction of a nitrogen at the 8-position of the tricyclic core resulted in active analogues with improved properties (aqueous solubility, protein binding and log D) and excellent rat pharmacokinetics (e.g., rat oral bioavailability of 89% for compound 17).

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