91-40-7
Product Name:
N-Phenylanthranilic acid
Formula:
C13H11NO2
Synonyms:
2-(Phenylamino)benzoic acid;Diphenylamine-2,2′-dicarboxylic acid;Diphenylamine-2-carboxylic acid;DpC;N-Phenylanthranilic acid
Inquiry
CHEMICAL AND PHYSICAL PROPERTIES
Physical Description | Solid; [Merck Index] Off-white powder; [Alfa Aesar MSDS] |
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Vapor Pressure | 0.00000238 [mmHg] |
Collision Cross Section | 144.5 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards] |
Chemical Classes | Nitrogen Compounds -> Aminobenzoic Acids |
SAFETY INFORMATION
Signal word | Warning |
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Pictogram(s) |
Exclamation Mark Irritant GHS07 |
GHS Hazard Statements |
H315:Skin corrosion/irritation H319:Serious eye damage/eye irritation H335:Specific target organ toxicity, single exposure;Respiratory tract irritation |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P264:Wash hands thoroughly after handling. P264:Wash skin thouroughly after handling. P280:Wear protective gloves/protective clothing/eye protection/face protection. P304+P340:IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. P405:Store locked up. |
COMPUTED DESCRIPTORS
Molecular Weight | 213.23 g/mol |
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XLogP3 | 4.4 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 3 |
Exact Mass | 213.078978594 g/mol |
Monoisotopic Mass | 213.078978594 g/mol |
Topological Polar Surface Area | 49.3 Ų |
Heavy Atom Count | 16 |
Formal Charge | 0 |
Complexity | 236 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently-Bonded Unit Count | 1 |
Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
Fenamic acid is an aminobenzoic acid that is the N-phenyl derivative of anthranilic acid. It acts as a parent skeleton for the synthesis of several non-steroidal anti-inflammatory drugs. It has a role as a membrane transport modulator. It is a secondary amino compound and an aminobenzoic acid. It is functionally related to an anthranilic acid.