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About This Item
Linear Formula:
IC6H3(CH3)CO2H
CAS Number:
Molecular Weight:
262.04
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
Assay
97%
mp
150-153 °C (lit.)
SMILES string
Cc1cccc(C(O)=O)c1I
InChI
1S/C8H7IO2/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4H,1H3,(H,10,11)
InChI key
PZUXUOZSSYKAMX-UHFFFAOYSA-N
Application
2-Iodo-3-methylbenzoic acid may be used in the synthesis of:
- methyl 2-iodo-3-methylbenzoate
- 10,11-dihydro-10-oxodibenz[b,f]oxepin-4-acetic acid
- 5-methyl-3-pentyl-1H-isochromen-1-one
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Asymmetric allylic oxidation with biarylbisoxazoline-copper (I) catalysis.
Andrus MB and Asgari D.
Tetrahedron, 56(32), 5775-5780 (2000)
Veronika Hampl et al.
Scientia pharmaceutica, 79(1), 21-30 (2011-05-28)
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 corresponding dihydroisocoumarins. A 4-chloroisocoumarin was prepared on an alternative pathway. Some of the new
G W Rewcastle et al.
Journal of medicinal chemistry, 34(2), 491-496 (1991-02-01)
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, in an effort to extend the structure-activity relationships for this series. As
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