2-Iodo-3-methylbenzoic acid

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Names

[ CAS No. ]:
108078-14-4

[ Name ]:
2-Iodo-3-methylbenzoic acid

[Synonym ]:
2-IODO-M-TOLUIC ACID
2-Iodo-3-methylbenzoic acid
2-Jod-m-toluylsaeure
3-methyl-2-iodobenzoic acid
MFCD00079764
Benzoic acid, 2-iodo-3-methyl-
1-iodo-3-methylbenzoic acid
2-Jod-3-methyl-benzoesaeure
2-iodo-3-methyl benzoic acid

Chemical & Physical Properties

[ Density]:
1.9±0.1 g/cm3

[ Boiling Point ]:
323.5±30.0 °C at 760 mmHg

[ Melting Point ]:
150-153 °C(lit.)

[ Molecular Formula ]:
C8H7IO2

[ Molecular Weight ]:
262.044

[ Flash Point ]:
149.5±24.6 °C

[ Exact Mass ]:
261.949066

[ PSA ]:
37.30000

[ LogP ]:
2.62

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.646

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2916399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 2-Amino-3-methylbenzoic acid
  • 3-Methyl-2-nitrobenzoic acid
  • 3-Methylbenzoic acid
  • 3-methyl-2-nitrobenzamide
  • 3-CYANO-2-NITROTOLUENE

DownStream

  • [1,1'-Biphenyl]-2,2'-dimethanol,6,6'-dimethyl-
  • 3-IODO-4-METHYLBENZYL ALCOHOL
  • Dimethyl Benzylmalonate
  • 2-Anilino-3-methylbenzoic acid

Customs

[ HS Code ]: 2916399090

[ Summary ]:
2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

New substituted isocoumarins and Dihydroisocoumarins and their cytotoxic activities.

Sci. Pharm. 79(1) , 21-30, (2011)

New isocoumarins were prepared in an efficient way from 2-iodobenzoic acid derivatives and hept-1-yne in a Sonogashira reaction, followed by spontaneous cyclization. Catalytic hydrogenation gave the c...

Potential antitumor agents. 62. Structure-activity relationships for tricyclic compounds related to the colon tumor active drug 9-oxo-9H-xanthene-4-acetic acid.

J. Med. Chem. 34(2) , 491-6, (1991)

A series of tricyclic analogues of 9-oxo-9H-xanthene-4-acetic acid have been prepared and evaluated for their ability to cause hemorrhagic necrosis in subcutaneously implanted colon 38 tumors in mice,...

Asymmetric allylic oxidation with biarylbisoxazoline-copper (I) catalysis. Andrus MB and Asgari D.

Tetrahedron 56(32) , 5775-5780, (2000)


More Articles

Related Compounds

  • 2-fluoro-6-iodo-3-methylbenzoic acid
  • 2-amino-5-iodo-3-methylbenzoic acid
  • 2-Amino-5-iodo-3-methylbenzoic Acid Methyl Ester
  • 2,5-Difluoro-4-iodo-3-methyl-benzoic acid
  • 4-Iodo-3-methylbenzoic acid
  • 4-Iodo-3-Methylbenzoic Acid Ethyl Ester
  • tert-butyl N-[2-amino-3-(5-bromothiophen-3-yl)propyl]carbamate
  • 2-(Bromomethyl)-1,3-dimethoxy-5-methylbenzene
  • 5-{1-[(aminooxy)methyl]cyclopropyl}-N,N,4-trimethyl-1,3-thiazol-2-amine
  • 3-Hydroxy-3-(2-methoxypyridin-3-yl)propanoic acid
  • 1-(3-Bromoprop-1-en-2-yl)-1,2,3,4-tetrahydronaphthalene
  • 1-{2-[2-(Propan-2-yl)-1,3-thiazol-4-yl]ethyl}cyclopropan-1-ol
  • tert-butyl N-[4-(4-oxobutyl)cyclohexyl]carbamate
  • tert-butyl N-[4-methyl-1-(piperazin-1-yl)pentan-3-yl]carbamate
  • 1-[1-(1,4-dimethyl-1H-pyrazol-3-yl)cyclopropyl]cyclopropan-1-amine
  • 3-[(Azetidin-1-yl)methyl]-5-chlorobenzonitrile
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