2-Methyl-1H-indole-3-carbaldehyde

Suppliers

Names

[ Name ]:
2-Methyl-1H-indole-3-carbaldehyde

[Synonym ]:
Indole-3-carboxaldehyde, 2-methyl-
3-FORMYL-2-METHYLINDOLE
2-Methylindole-3-carboxaldehyde
2-Methyl-1H-indole-3-carbaldehyde
MFCD00012077
EINECS 226-512-6
1H-Indole-3-carboxaldehyde, 2-methyl-

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
344.3±22.0 °C at 760 mmHg

[ Melting Point ]:
200-201 °C(lit.)

[ Molecular Formula ]:
C₁₀H₉NO

[ Molecular Weight ]:
159.185

[ Flash Point ]:
169.9±29.8 °C

[ Exact Mass ]:
159.068420

[ PSA ]:
32.86000

[ LogP ]:
2.14

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.699

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S37/39-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

2-Methylindole
N,N-Dimethylformamide
N-Methylaniline
2-bromo-1H-indole-3-carbaldehyde
Tetramethyltin
TRIMETHYL(3-PYRIDYL)TIN
2-(Trimethylstannyl)pyridine
Chloroform
HYDROGEN CYANIDE

DownStream

2-Methyl-1H-indole-3-carbonitrile
ethyl 2-(3-formyl-2-methylindol-1-yl)acetate
1,2-DIMETHYL-1H-INDOLE-3-CARBOXALDEHYDE
methyl 1,2-dimethyl-1H-indole-3-carboxylate
1-ALLYL-2-METHYL-1H-INDOLE-3-CARBALDEHYDE
ETHYL BETA-CARBOLINE-3-CARBOXYLATE
(E)-2-methyl-3-(2-nitrovinyl)-1H-indole
2,3-Dimethyl-1H-indole
N-Acetylanthranilic acid
2-Methyl-1H-indole-3-carboxylic acid

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Synthesis and antifungal activity of novel streptochlorin analogues.

Eur. J. Med. Chem. 92 , 776-83, (2015)

Streptochlorin, first isolated as a new antibiotic in 1988 from the lipophilic extracts of the mycelium of a Streptomyces sp, is an indole natural products with a variety of biological activities. Bas...

Functionalization of benzylic C(sp(3))-H bonds of heteroaryl aldehydes through N-heterocyclic carbene organocatalysis.

Angew. Chem. Int. Ed. Engl. 52(42) , 11134-7, (2013)

Aryl aldehyde activation: Oxidative activation of 2-methylindole-3-carboxaldehyde (I) through N-heterocyclic carbene (NHC) organocatalysis generates heterocyclic ortho-quinodimethane (II) as a key int...

(2-Methyl-1-phenyl-sulfonyl-1H-indol-3-yl)methanol.

Acta Crystallogr. Sect. E Struct. Rep. Online 64(2) , o542-o542, (2008)

In the title compound, C(16)H(15)NO(3)S, the plane of the phenyl ring forms a dihedral angle of 80.37 (8)° with the indole ring system. The crystal packing is stabilized by weak O-H⋯O hydrogen bonds w...

5-Ethyl-2-methyl-1H-indole-3-carbaldehyde
1-ETHYL-2-METHYL-1H-INDOLE-3-CARBALDEHYDE
5-Bromo-2-methyl-1H-indole-3-carbaldehyde
6-Bromo-2-methyl-1H-indole-3-carbaldehyde
5-nitro-2-methyl-1H-indole-3-carbaldehyde
1-ALLYL-2-METHYL-1H-INDOLE-3-CARBALDEHYDE
2-(1-Methylpyrrolidin-2-yl)pyrimidine-4-carboxylic acid
N,N-dimethyl-5-(piperidin-4-yl)-1,3-thiazol-2-amine
1-[(4-Methylthiophen-3-yl)methyl]cyclopropan-1-amine
4-[2-(4-bromophenyl)ethyl]-1H-pyrazole
8-bromo-N-(pentan-2-yl)quinazolin-2-amine
O-[2-(1-methyl-1H-1,2,3-triazol-4-yl)propan-2-yl]hydroxylamine
{1-[(2-Bromo-5-methylphenyl)methyl]cyclopropyl}methanol
4-Chloro-2-methyl-6-{[(prop-2-en-1-yloxy)carbonyl]amino}benzoic acid
[2-(2-tert-butyl-2H-1,2,3,4-tetrazol-5-yl)propan-2-yl](methyl)amine
N-{1-[(methylcarbamoyl)methyl]piperidin-4-yl}cyclobutanecarboxamide

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