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

Modify Date: 2024-01-03 12:16:16

2-Methyl-1H-indole-3-carbaldehyde structure	Common Name	2-Methyl-1H-indole-3-carbaldehyde
	CAS Number	5416-80-8	Molecular Weight	159.185
	Density	1.2±0.1 g/cm3	Boiling Point	344.3±22.0 °C at 760 mmHg
	Molecular Formula	C₁₀H₉NO	Melting Point	200-201 °C(lit.)
	MSDS	Chinese USA	Flash Point	169.9±29.8 °C
	Symbol	GHS07	Signal Word	Warning

Name	2-Methylindole-3-carboxaldehyde
Synonym	More Synonyms

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

2-Methyl-1H-indole-3-carbaldehyde MSDS(Chinese)

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

Precursor 9
CAS#:95-20-5 2-Methylindole CAS#:68-12-2 N,N-Dimethylfor... CAS#:100-61-8 N-Methylaniline CAS#:119910-45-1 2-bromo-1H-indo...
CAS#:594-27-4 Tetramethyltin CAS#:59020-09-6 TRIMETHYL(3-PYR... CAS#:13737-05-8 2-(Trimethylsta... CAS#:67-66-3 Chloroform
CAS#:74-90-8 HYDROGEN CYANIDE
DownStream 10
CAS#:51072-83-4 2-Methyl-1H-ind... CAS#:433307-59-6 ethyl 2-(3-form... CAS#:38292-40-9 1,2-DIMETHYL-1H... CAS#:54109-65-8 methyl 1,2-dime...
CAS#:230283-19-9 1-ALLYL-2-METHY... CAS#:74214-62-3 ETHYL BETA-CARB... CAS#:2826-91-7 (E)-2-methyl-3-... CAS#:91-55-4 2,3-Dimethyl-1H...
CAS#:89-52-1 N-Acetylanthran... CAS#:63176-44-3 2-Methyl-1H-ind...

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%

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...

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-