N-(4-TRIFLUOROMETHOXYPHENYL)ANTHRANILIC ACID

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Names

[ CAS No. ]:
51679-41-5

[ Name ]:
N-(4-TRIFLUOROMETHOXYPHENYL)ANTHRANILIC ACID

[Synonym ]:
Benzoic acid,2-((4-(trifluoromethoxy)phenyl)amino)
N-(p-Trifluoromethoxyphenyl)anthranilic acid
Anthranilic acid,N-(p-trifluoromethoxyphenyl)

Chemical & Physical Properties

[ Density]:
1.426 g/cm3

[ Boiling Point ]:
379ºC at 760 mmHg

[ Molecular Formula ]:
C14H10F3NO3

[ Molecular Weight ]:
297.22900

[ Flash Point ]:
183ºC

[ Exact Mass ]:
297.06100

[ PSA ]:
58.56000

[ LogP ]:
4.10000

[ Index of Refraction ]:
1.583

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CB4290000
CHEMICAL NAME :
Anthranilic acid, N-(p-trifluoromethoxyphenyl)-
CAS REGISTRY NUMBER :
51679-41-5
LAST UPDATED :
199803
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C14-H10-F3-N-O3
MOLECULAR WEIGHT :
297.25
WISWESSER LINE NOTATION :
QVR BMR DOXFFF

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
140 mg/kg
TOXIC EFFECTS :
Biochemical - Metabolism (Intermediary) - effect on inflammation or mediation of inflammation
REFERENCE :
PCJOAU Pharmaceutical Chemistry Journal (English Translation). Translation of KHFZAN. (Plenum Pub. Corp., 233 Spring St., New York, NY 10013) No.1- 1967- Volume(issue)/page/year: 7,755,1973

Safety Information

[ HS Code ]:
2922509090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • methyl 2-[4-(trifluoromethoxy)anilino]benzoate
  • 4-(Trifluoromethoxy)aniline
  • Methyl 2-iodobenzoate
  • 2-Bromobenzoic acid

DownStream

  • 9-chloro-2-(trifluoromethoxy)acridine

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Related Compounds

  • N-(4-TRIFLUOROMETHYLPHENYL)ANTHRANILIC ACID
  • N-(4-CHLOROPHENYL)ANTHRANILIC ACID
  • N-(4-Biphenylyl)anthranilic acid
  • N-(4-chlorophenyl)anthranilic acid methyl ester
  • N-(4-FLUOROPHENYL)ANTHRANILIC ACID
  • N-(4-tert-butylphenyl)anthranilic acid methyl ester
  • 4-(1H-benzo[d]imidazol-2-yl)-N,N-dimethylpiperidine-1-sulfonamide
  • (2-Chloro-7-methylquinolin-3-yl)methyl 2-chloropyridine-3-carboxylate
  • 1-[(4-Methylphenyl)carbamoyl]ethyl 2-chloropyridine-3-carboxylate
  • 2-(9H-fluoren-3-yl)-2-oxoethyl 2-chloropyridine-3-carboxylate
  • 1-[(2,5-Dichlorophenyl)carbamoyl]ethyl 2-chloropyridine-3-carboxylate
  • [2-[2,5-Dimethyl-1-[3-(trifluoromethyl)phenyl]pyrrol-3-yl]-2-oxoethyl] 2-chloropyridine-3-carboxylate
  • ({3-[(2-Chlorophenyl)methyl]-2,3-dihydro-1,3-thiazol-2-ylidene}carbamoyl)methyl 2-chloropyridine-3-carboxylate
  • [(2lambda4,1,3-Benzothiadiazol-4-yl)carbamoyl]methyl 2-chloropyridine-3-carboxylate
  • {[3-(Ethoxycarbonyl)-4-(furan-2-YL)thiophen-2-YL]carbamoyl}methyl 2-chloropyridine-3-carboxylate
  • [(9,10-Dioxo-9,10-dihydroanthracen-1-yl)carbamoyl]methyl 2-chloropyridine-3-carboxylate
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