N-(3-Chloro-ortho-tolyl)anthranilic acid

• CAS: 13710-19-5
• Catalog Number: ACM13710195
• Category: Other Products
• Molecular Weight: 261.7
• Molecular Formula: C₁₄H₁₂ClNO₂
• Synonyms: CLOTAM;LABOTEST-BB LT00772313;2-(3-CHLORO-O-TOLUIDINO)BENZOIC ACID;2 (3-CHLORO-2-METHYLANILINO)BENZOIC ACID;2-[(3-CHLORO-2-METHYLPHENYL)AMINO]BENZOIC ACID;TOLFENAMIC ACID;2-((3-chloro-2-methylphenyl)amino)-benzoicaci;gea6414
• Melting Point: 210-214°C
• Hazard Statements: Xn
• Supplemental Hazard Statements: H301
• Symbol: GHS06

Custom Q&A

What is the molecular formula of tolfenamic acid?

The molecular formula of tolfenamic acid is C14H12ClNO2.

What is the molecular weight of tolfenamic acid?

The molecular weight of tolfenamic acid is 261.70 g/mol.

What is another name for tolfenamic acid?

Another name for tolfenamic acid is Clotam.

What is the IUPAC name of tolfenamic acid?

The IUPAC name of tolfenamic acid is 2-(3-chloro-2-methylanilino)benzoic acid.

What is the InChIKey of tolfenamic acid?

The InChIKey of tolfenamic acid is YEZNLOUZAIOMLT-UHFFFAOYSA-N.

What is the CAS number of tolfenamic acid?

The CAS number of tolfenamic acid is 13710-19-5.

What is the EC number of tolfenamic acid?

The EC number of tolfenamic acid is 237-264-3.

What is the ChEMBL ID of tolfenamic acid?

The ChEMBL ID of tolfenamic acid is CHEMBL121626.

What is the UNII of tolfenamic acid?

The UNII of tolfenamic acid is 3G943U18KM.

What is the therapeutic application of tolfenamic acid?

Tolfenamic acid is used for relieving the pain of migraine and also shows anticancer activity. It is a non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory, antipyretic, analgesic, and potential anti-neoplastic activities.

Synthetic Use

Upstream Synthesis Route 1

• 87-60-5
• 118-91-2

• 13710-19-5

Reference: [1] Patent: CN104557584, 2016, B, . Location in patent: Paragraph 0016; 0017; 0018

Upstream Synthesis Route 2

• 12775-96-1
• 87-60-5
• 88-65-3

• 13710-22-0
• 13710-19-5

Reference: [1] Patent: US4092430, 1978, A,

Upstream Synthesis Route 3

• 16497-87-3
• 87-60-5

• 13710-19-5

Reference: [1] Chemistry and Biodiversity, 2009, vol. 6, # 6, p. 948 - 960
[2] Arzneimittel-Forschung/Drug Research, 1983, vol. 33, # 4 A, p. 621 - 627

Upstream Synthesis Route 4

• 16497-87-3
• 87-60-5

• 13710-19-5

Reference: [1]Chemistry and biodiversity,2009,vol. 6,p. 948 - 960
[2]Arzneimittel-Forschung/Drug Research,1983,vol. 33,p. 621 - 627