| Identification | More | [Name]
1-Methylindole-2-carboxylic acid | [CAS]
16136-58-6 | [Synonyms]
1-METHYL-1H-INDOLE-2-CARBOXYLIC ACID
1-METHYLINDOLE-2-CARBOXYLIC ACID
AKOS JY2082906
N-METHYL-2-INDOLECARBOXYLIC ACID
RARECHEM AL BE 0864
1H-Indole-2-carboxylic acid, 1-methyl-
1-methyl-1h-indole-2-carboxylicaci
1-Methyl-2-indolecarboxylic acid
1-methyl-2-indolecarboxylicacid
Indole-2-carboxylic acid, 1-methyl-
1-Methylindole-2-CarboxylicAcid97%
1-Me-ICA
1-Methylindole-2-carboxylic acid, 1-Methyl-1H-indole-2-carboxylic acid, 99% | [Molecular Formula]
C10H9NO2 | [MDL Number]
MFCD00005801 | [Molecular Weight]
175.18 | [MOL File]
16136-58-6.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [RTECS ]
NL6012400
| [HazardClass ]
IRRITANT | [HS Code ]
29339980 |
| Hazard Information | Back Directory | [Chemical Properties]
Beige crystalline powder | [Uses]
• ;Reactant for preparation of keto-indoles as novel indoleamine 2,3-dioxygenase (IDO) inhibitors1• ;Reactant for synthesis of fenbufen and ethacrynic acid derivatives as potential antitumor agents via amide coupling reactions2• ;Reactant for diastereoselective synthesis of vinylated heterocycles via ruthenium-catalyzed oxidative vinylation with alkenes3• ;Reactant for synthesis of 2,3-dihalo indoles via hypervalent iodine mediated decarboxylative halogenation4• ;Reactant for preparation of α-ketoamides as cathepsin S inhibitors with potential applications ag | [Uses]
- Reactant for preparation of keto-indoles as novel indoleamine 2,3-dioxygenase (IDO) inhibitors
- Reactant for synthesis of fenbufen and ethacrynic acid derivatives as potential antitumor agents via amide coupling reactions
- Reactant for diastereoselective synthesis of vinylated heterocycles via ruthenium-catalyzed oxidative vinylation with alkenes
- Reactant for synthesis of 2,3-dihalo indoles via hypervalent iodine mediated decarboxylative halogenation
- Reactant for preparation of α-ketoamides as cathepsin S inhibitors with potential applications against tumor invasion and angiogenesis
- Reactant for preparation of anthranilic acid mimics as bacterial translation inhibitors
| [General Description]
1-Methylindole-2-carboxylic acid reacts with thionyl chloride to yield sulfinyl chlorides. |
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