2-[(2-AMINO-4-PYRIMIDINYL)AMINO]BENZOIC ACID

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Names

[ CAS No. ]:
31185-78-1

[ Name ]:
2-[(2-AMINO-4-PYRIMIDINYL)AMINO]BENZOIC ACID

[Synonym ]:
N-(6-(2-Aminopyrimidinyl))anthranilic acid
N-(2-amino-pyrimidin-4-yl)-anthranilic acid
N-(2-Amino-pyrimidin-4-yl)-anthranilsaeure
ANTHRANILIC ACID,N-(6-(2-AMINOPYRIMIDINYL))
2-(2-amino-pyrimidin-4-ylamino)-benzoic acid

Chemical & Physical Properties

[ Density]:
1.468g/cm3

[ Boiling Point ]:
530.2ºC at 760 mmHg

[ Molecular Formula ]:
C11H10N4O2

[ Molecular Weight ]:
230.22300

[ Flash Point ]:
274.4ºC

[ Exact Mass ]:
230.08000

[ PSA ]:
105.09000

[ LogP ]:
0.85260

[ Index of Refraction ]:
1.736

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CB2540000
CHEMICAL NAME :
Anthranilic acid, N-(6-(2-aminopyrimidinyl))-
CAS REGISTRY NUMBER :
31185-78-1
BEILSTEIN REFERENCE NO. :
0216806
LAST UPDATED :
199612
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C11-H10-N4-O2
MOLECULAR WEIGHT :
230.25
WISWESSER LINE NOTATION :
T6N CNJ BZ DMR BVQ

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 :
680 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
RPTOAN Russian Pharmacology and Toxicology (English Translation). Translation of FATOAO. (Euromed Pub., 33, Woodlands Rd., Surbiton, Surrey, UK) V.30- 1967- Volume(issue)/page/year: 37,105,1974

Safety Information

[ HS Code ]:
2933599090

Synthetic Route

Precursor & DownStream

Precursor

  • 2-Amino-4-chloropyrimidine
  • Anthranilic acid

DownStream

Customs

[ HS Code ]: 2933599090

[ Summary ]:
2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%


Related Compounds

  • 2-[(2-Amino-6-methyl-4-pyrimidinyl)amino]benzoic acid
  • 2-Amino-4-(p-carboxyanilino)-6-methylpyrimidine
  • 2-[(2-aminopyrimidin-4-yl)carbamoyl]benzoic acid
  • decahydro-4a-hydroxy-4-oxo-2-propyl-5-vinylquinoline-1-carboxylic acid phenyl ester
  • 2-(2-amino-4-methoxy-phenylsulfanyl)-benzoic acid methyl ester
  • 2-(2-amino-4-methoxyphenylsulfanyl)benzoic acid
  • 2-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methylpentanamido]-2-methylbutanoic acid
  • 4-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pent-4-ynoyl]morpholine-2-carboxylic acid
  • 2-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanamido]-4,4,4-trifluorobutanoic acid
  • (2S,4S)-1-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanoyl]-4-hydroxypyrrolidine-2-carboxylic acid
  • 5-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanamido]pyridine-3-carboxylic acid
  • (2S)-2-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanamido]-3-methylpentanoic acid
  • 3-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-N,2,2,3-tetramethylbutanamido]-2-methylpropanoic acid
  • 4-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2,3-trimethylbutanamido]-3-methoxybutanoic acid
  • (2S)-2-{4-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)ethyl]-N,5-dimethylhexanamido}propanoic acid
  • 3-{[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-fluorophenyl]formamido}-2-methylbutanoic acid
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