Indole-7-carboxylic acid, 97%
Indole-7-carboxylic acid, 97%
Indole-7-carboxylic acid, 97%
Thermo Scientific Chemicals

Indole-7-carboxylic acid, 97%

CAS: 1670-83-3 | C9H7NO2 | 161.16 g/mol
製品番号(カタログ番号) H54931.03
または、製品番号H54931-03
価格(JPY)
-
数量:
1 g
一括またはカスタム形式をリクエストする
仕様
CAS1670-83-3
化学物質名または材質Indole-7-carboxylic acid
EINECS番号216-801-5
式量161.05
健康被害1Warning
さらに表示
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.
RUO – Research Use Only

General References:

  1. 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.
  2. 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.