CAS 5416-80-8|2-Methyl-1H-indole-3-carbaldehyde

Introduction：Basic information about CAS 5416-80-8|2-Methyl-1H-indole-3-carbaldehyde, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Chemical & Physical Properties
3. Safety Information
4. Customs
5. Articles3
6. Synonyms

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	ChineseUSA	Flash Point	169.9±29.8 °C
Symbol	GHS07	Signal Word	Warning

Names

Name	2-Methylindole-3-carboxaldehyde
Synonym	More Synonyms

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
InChIKey	CYZIVXOEJNAIBS-UHFFFAOYSA-N
SMILES	Cc1[nH]c2ccccc2c1C=O

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

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%

Articles3

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...

Synonyms

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-

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