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ChemicalBook--->CAS DataBase List--->16136-58-6

16136-58-6

16136-58-6 Structure

16136-58-6 Structure
IdentificationMore
[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
Chemical PropertiesBack Directory
[Appearance]

Beige crystalline powder
[Melting point ]

212-213 °C (dec.) (lit.)
[Boiling point ]

389.0±15.0 °C(Predicted)
[density ]

1.24±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

Crystalline Powder
[pka]

4.19±0.30(Predicted)
[color ]

Beige
[CAS DataBase Reference]

16136-58-6(CAS DataBase Reference)
[NIST Chemistry Reference]

1-Methylindole-2-carboxylic acid(16136-58-6)
Safety DataBack 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 InformationBack 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.
Spectrum DetailBack Directory
[Spectrum Detail]

1-Methylindole-2-carboxylic acid(16136-58-6)MS
1-Methylindole-2-carboxylic acid(16136-58-6)1HNMR
1-Methylindole-2-carboxylic acid(16136-58-6)IR1
1-Methylindole-2-carboxylic acid(16136-58-6)IR2
1-Methylindole-2-carboxylic acid(16136-58-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

1-Methylindole-2-carboxylic acid(16136-58-6)
[Sigma Aldrich]

16136-58-6(sigmaaldrich)
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