2-Benzamido-5-chlorobenzoic acid

Base Information

• Chemical Name: 2-Benzamido-5-chlorobenzoic acid
• CAS No.: 19407-45-5
• Molecular Formula: C14H10ClNO3
• Molecular Weight: 275.691
• Hs Code.: 2924299090
• European Community (EC) Number: 922-761-6
• DSSTox Substance ID: DTXSID90424216
• Wikidata: Q82236695
• Mol file: 19407-45-5.mol

Synonyms:2-benzamido-5-chlorobenzoic acid;19407-45-5;2-Benzamido-5-chlorobenzoicacid;SCHEMBL6351321;DTXSID90424216;2-benzamido-5-chloro benzoic acid;STK292628;AKOS000134432;SDCCGSBI-0139278.P001;CS-0359070;5-chloro-2-[(phenylcarbonyl)amino]benzoic acid;I11759

Chemical Property of 2-Benzamido-5-chlorobenzoic acid

Chemical Property:

• PSA: 69.89000
• LogP: 3.67450
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: 4.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 275.0349209
• Heavy Atom Count: 19
• Complexity: 342

Purity/Quality:

97% ^*data from raw suppliers

2-Benzamido-5-chlorobenzoicacid 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(=O)NC2=C(C=C(C=C2)Cl)C(=O)O

Technology Process of 2-Benzamido-5-chlorobenzoic acid

There total 5 articles about 2-Benzamido-5-chlorobenzoic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 83.0%

benzoyl chloride (98-88-4) + 5-chloroanthranilic acid (635-21-2) → 2-benzamido-5-chlorobenzoic acid (19407-45-5)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; for 3h;

DOI:10.1080/00397911.2014.910529

Reference yield: 74.0%

5-chloro-2-phenylindole (23746-76-1) → 2-benzamido-5-chlorobenzoic acid (19407-45-5)

Guidance literature:

With tert.-butylhydroperoxide; In water; chlorobenzene; at 125 ℃; for 16h;

DOI:10.1039/c9ob00797k

Reference yield: 4.0%

6-chloro-2-phenylquinolin-4(1H)-one (112182-50-0) → methyl 2-benzamido-5-chlorobenzoate (100865-38-1) + 2-benzamido-5-chlorobenzoic acid (19407-45-5) + (5-chlorobenzo[c]isoxazol-3-yl)(phenyl)methanone + 6-chloro-2-phenyl-benzo[d][1,3]oxazin-4-one (7033-51-4)

Guidance literature:

With sodium hydroxide; sode de l'acide trichloroisocyanurique; In methanol;

DOI:10.1039/P19930000511

upstream raw materials:

methanol

6-chloro-2-phenylquinolin-4(1H)-one

benzoyl chloride

5-chloroanthranilic acid

Downstream raw materials:

6-chloro-3-(3-chloro-4-fluorophenyl)-2-phenylquinazolin-4(3H)-one

C₂₁H₁₄ClFN₂O

C₂₁H₁₄Cl₂N₂O

6-chloro-3-(4-fluorophenyl)-2-phenylquinazolin-4(3H)-one

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