Methyl 4-amino-3-iodobenzoate

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Names

[ CAS No. ]:
19718-49-1

[ Name ]:
Methyl 4-amino-3-iodobenzoate

[Synonym ]:
Methyl 4-amino-3-iodobenzoate
2-iodo-4-(methoxycarbonyl)aniline
methyl 4-amino-3-iodo-benzoate
4-methoxycarbonyl-2-iodoaniline
4-Amino-3-iodo-benzoic acid methyl ester
MFCD00090423
Benzoic acid, 4-amino-3-iodo-, methyl ester

Chemical & Physical Properties

[ Density]:
1.8±0.1 g/cm3

[ Boiling Point ]:
369.6±32.0 °C at 760 mmHg

[ Melting Point ]:
86-91 °C(lit.)

[ Molecular Formula ]:
C8H8INO2

[ Molecular Weight ]:
277.059

[ Flash Point ]:
177.3±25.1 °C

[ Exact Mass ]:
276.959961

[ PSA ]:
52.32000

[ LogP ]:
2.85

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.648

[ Storage condition ]:
2-8°C

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

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922499990

Precursor & DownStream

Precursor

  • Methyl 4-aminobenzoate
  • Methyl 3-Amino-4-nitrobenzoate
  • 4-Aminobenzoic acid
  • Methanol
  • 4-Amino-3-iodobenzoic acid

DownStream

  • methyl 4-acetamido-3-iodobenzoate
  • Methyl 3-iodobenzoate
  • Methyl indole-5-carboxylate
  • methyl cinnoline-6-carboxylate
  • Methyl 4-aminobenzoate
  • Methyl 2-oxo-1,2,3,4-tetrahydroquinoline-6-​carboxylate
  • 4-Amino-3-iodobenzoic acid
  • 4-azido-3-iodobenzoic acid
  • methyl 3-iodo-4-(pyrrolidin-1-yldiazenyl)benzoate
  • Methyl 3-iodo-4-(methylamino)benzoate

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

C-N bond formation via Cu-catalyzed cross-coupling with boronic acids leading to methyl carbazole-3-carboxylate: synthesis of carbazole alkaloids. Rasheed SK, et al.

RSC Advances 4(10) , 4960-4969, (2014)

Solid-phase synthesis of an AB loop mimetic of the Ce3 domain of human IgE: Macrocyclization by Sonogashira coupling. Spivey AC, et al.

J. Org. Chem. 68(5) , 1843-1851, (2003)

Targeting aldehyde dehydrogenase: a potential approach for cell labeling. Vaidyanathan G, et al.

Nucl. Med. Biol. 36(8) , 919-929, (2009)


More Articles

Related Compounds

  • Methyl 4-amino-3-fluoro-5-iodobenzoate
  • Methyl 4-amino-3-chloro-5-nitrobenzoate
  • methyl 4-amino-3-chloro-6-(3,4-dimethylphenyl)pyridine-2-carboxylate
  • Methyl 4-amino-3-iodo-5-methylbenzoate
  • methyl 4-amino-3-methyl-5-methylthiomethylbenzoate
  • Methyl 4-amino-3-(methylamino)benzoate
  • 1-Benzyl-5-methyl-1H-indole-3-carbonitrile
  • 1H-Indole-3-carbonitrile, 1-[2-(1-piperidinyl)ethyl]-5-propyl-
  • (4-Chloro-3-methylphenyl)methanethiol
  • 1-(2-Methyl-4-methylene-2-phenylcyclopentyl)ethanone
  • 4-(4-Chlorophenyl)-1-(4-methyl-1H-imidazol-1-yl)-2-butanone
  • 1-allyl-3-(tetrahydro-2H-pyran-4-yl)urea
  • 4-(4-(Methoxycarbonyl)piperidin-1-yl)benzoic acid
  • Methyl 1-(2-aminophenyl)piperidine-4-carboxylate
  • 3-(4-fluoro-1H-indol-3-yl)-2-oxopropanoic acid
  • 4-Fluoro-3-methanesulfonylmethyl-phenylamine
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