Methyl 2-amino-3,5-dibromobenzoate

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Names

[ CAS No. ]:
606-00-8

[ Name ]:
Methyl 2-amino-3,5-dibromobenzoate

[Synonym ]:
2-Amino-3,5-dibrom-benzoesaeure-methylester
Methyl 3,5-dibromoanthranilate
EINECS 400-990-8
3,5-Dibromoanthranilic Acid Methyl Ester
Anthranilic acid,3,5-dibromo-,methyl ester
MFCD00010873
2-Amino-3,5-dibromobenzoic Acid Methyl Ester
3.5-Dibrom-anthranilsaeuremethylester

Chemical & Physical Properties

[ Density]:
1.907 g/cm3

[ Boiling Point ]:
317.9ºC at 760 mmHg

[ Melting Point ]:
89-91 °C(lit.)

[ Molecular Formula ]:
C8H7Br2NO2

[ Molecular Weight ]:
308.95500

[ Flash Point ]:
146.1ºC

[ Exact Mass ]:
306.88400

[ PSA ]:
52.32000

[ LogP ]:
3.16160

[ Index of Refraction ]:
1.63

[ Storage condition ]:
2~8°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36/37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922499990

Precursor & DownStream

Precursor

  • Methyl 2-aminobenzoate
  • diazomethane
  • 2-Amino-3,5-dibromobenzoic acid
  • Dimethyl sulfate
  • Methyl 2-amino-5-bromobenzoate

DownStream

  • Methyl 3,5-dibromobenzoate
  • Benzoic acid,3,5-dibromo-2-chloro-
  • 3,5-Dibromobenzoic acid

Customs

[ HS Code ]: 2922499990

[ Summary ]:
HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

Articles

Cobalt (II) Schiff's base complex catalysed oxidation of alcohols with dioxygen in the presence of ethyl 2-oxocyclopentanecarboxylate. Punniyamurthy T and Iqbal J.

Tetrahedron Lett. 35(23) , 4007-10, (1994)

Cobalt catalysed allylic and benzylic oxidations with dioxygen in the presence of ethyl 2-oxocyclopentanecarboxylate. Punniyamurthy T and Iqbal J.

Tetrahedron Lett. 35(23) , 4003-6, (1994)

The chemistry of aryllead (IV) tricarboxylates. Reaction with ß-keto esters: a convenient route to a-arylated ketones. Pinhey JT and Rowe BA.

Aust. J. Chem. 33(1) , 113-20, (1980)


More Articles


Related Compounds

  • Methyl 2-aMino-3,5-dichlorobenzoate
  • Methyl 2-amino-3,5-dimethylbenzoate
  • methyl 2-amino-3,5-dimethoxybenzoate
  • methyl 2-amino-3,5-diiodobenzoate
  • Bromhexine hydrochloride
  • 2-Amino-2-methyl-hexadiin-(3,5)
  • 2-Bromo-3,4,5,6-tetramethoxybenzoic acid
  • 2-[3-(2S)-2-Aziridinylphenoxy]pyrimidine
  • N-(1,4-Dimethyl-2-naphthalenyl)acetamide
  • 1,1a(2)-Biphenyl, 2,2a(2),3-trifluoro-3a(2)-iodo-
  • 3-Hydroxy-4,5-dimethylbenzaldehyde oxime
  • 2,4-Dichlorobenzo[g]quinoline-5,10-dione
  • 3-Bromobicyclo[3.2.2]nona-3,6-dien-2-one
  • 4,5,6,7-Tetramethoxy-3(2H)-benzofuranone
  • 5-[2-(1-Naphthalenyl)diazenyl]pyrimidine
  • 5-(2-Chlorophenyl)-4-methyl-1H-imidazole
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