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ChemicalBook--->CAS DataBase List--->1074-88-0

1074-88-0

1074-88-0 Structure

1074-88-0 Structure
IdentificationMore
[Name]

Indole-7-carboxaldehyde
[CAS]

1074-88-0
[Synonyms]

1H-INDOLE-5-CARBALDEHYDE
1H-INDOLE-7-CARBALDEHYDE
7-FORMYLINDOLE
INDOLE-7-ALDEHYDE
INDOLE-7-CARBALDEHYDE
INDOLE-7-CARBOXALDEHYDE
RARECHEM AH BS 0111
7-Indolecarboxaldehyde
1H-Indole-7-carboxaldehyde (9CI)
INDOLE-7-CARBOXALDEHYDE (7-FORMYLINDOLE)
1H-Indole-7-carboxaldehyde
7-Formyl-1H-indole
[Molecular Formula]

C9H7NO
[MDL Number]

MFCD01318152
[Molecular Weight]

145.16
[MOL File]

1074-88-0.mol
Chemical PropertiesBack Directory
[Appearance]

Yellow Crystalline Solid
[Melting point ]

87-91 °C (lit.)
[Boiling point ]

339.1±15.0 °C(Predicted)
[density ]

1.278±0.06 g/cm3(Predicted)
[storage temp. ]

Keep Cold
[solubility ]

Chloroform, Dichloromethane
[form ]

Solid
[pka]

15.50±0.30(Predicted)
[color ]

Yellow Crystalline
[Water Solubility ]

insoluble
[Sensitive ]

Air Sensitive
[BRN ]

1524960
[CAS DataBase Reference]

1074-88-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R43:May cause sensitization by skin contact.
[Safety Statements ]

S36/37:Wear suitable protective clothing and gloves .
[WGK Germany ]

3
[F ]

10
[HS Code ]

29339900
Raw materials And Preparation ProductsBack Directory
[Raw materials]

N,N-Dimethylformamide-->Lithium Aluminum Hydride-->Manganese dioxide-->N,N-Dimethylformamide dimethyl acetal-->Titanous chloride-->3-Methyl-2-nitrobenzoic acid
[Preparation Products]

ethyl 3-(1H-indol-7-yl)propanoate-->7-ForMyl-1-Methyl-1H-indole-3-carbonitrile-->7-ForMyl-1H-indole-3-carbonitrile-->3-Iodo-1-methyl-1H-indole-7-carbaldehyde-->S-6-(tert-butoxycarbonyl)-5,6-dihydro-6H-[1,4]diazepino[6,7,1-hi]indole
Hazard InformationBack Directory
[Chemical Properties]

Yellow Crystalline Solid
[Uses]

Indole-7-carboxaldehyde (cas# 1074-88-0) is a compound useful in organic synthesis.
[Uses]

Indole-7-carboxaldehyde is used in an efficient synthesis of fused pyrroloquinolinedicarboxylates from acetylenedicarboxylates and triphenylphosphine. 1.reactant for preparation of antiandrogens. 2.reactant for preparation of antiplatelet agent. 3.reactant for preparation of liver
[Definition]

ChEBI: Indole-7-carboxaldehyde is a member of indoles.
[Synthesis Reference(s)]

Synthetic Communications, 36, p. 1051, 2006 DOI: 10.1080/00397910500503470
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Indole-7-carboxaldehyde, 98%(1074-88-0)
[Alfa Aesar]

Indole-7-carboxaldehyde, 98%(1074-88-0)
[Sigma Aldrich]

1074-88-0(sigmaaldrich)
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