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Thermo Scientific Chemicals
Indole-7-carboxylic acid, 97%
CAS: 1670-83-3 | C9H7NO2 | 161.16 g/mol
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Catalog number H54931.03
also known as H54931-03
Price (EUR)
40,50
Each
Quantity:
1 g
Price (EUR)
40,50
Each
Specifications
CAS1670-83-3
Chemical Name or MaterialIndole-7-carboxylic acid
EINECS Number216-801-5
Formula Weight161.05
Health Hazard 1Warning
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Indole-7-carboxylic acid is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Indole-7-carboxylic acid is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Solubility
Soluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
Indole-7-carboxylic acid is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Solubility
Soluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Yuji Enomoto.; Yoshio Furutani.; Hiroshi Naganawa.; Masa Hamada.; Tomio Takeuchi.; Hamao Umezawa. Studies on the total synthesis of CC-1065: preparation of a synthetic simplified 3-carbamoyl-1,2-dihydro-3H-pyrrolo[3,2-e]indole dimer/trimer/tetramer (CDPI dimer/trimer/tetramer) and development of methodology for PDE-I dimer methyl ester formation. J. Org. Chem. 1987, 52 (8), 1521-1530.
- Dale L. Boger.; Robert S. Coleman.; Benedict J. Invergo. Micellar system in copper-catalyzed hydroxylation of arylboronic acids: facile access to phenols. Chemical Communications. 2011, 47 (42), 11775-11777.