CAS 25365-71-3|2-phenylindole-3-carboxaldehyde

Introduction：Basic information about CAS 25365-71-3|2-phenylindole-3-carboxaldehyde, 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. Articles4
6. Synonyms

Common Name	2-phenylindole-3-carboxaldehyde
CAS Number	25365-71-3	Molecular Weight	221.25400
Density	1.237 g/cm3	Boiling Point	462.9ºC at 760 mmHg
Molecular Formula	C₁₅H₁₁NO	Melting Point	249-253 °C(lit.)
MSDS	ChineseUSA	Flash Point	237.5ºC
Symbol	GHS07	Signal Word	Warning

Names

Name	2-phenyl-1H-indole-3-carbaldehyde
Synonym	More Synonyms

Chemical & Physical Properties

Density	1.237 g/cm3
Boiling Point	462.9ºC at 760 mmHg
Melting Point	249-253 °C(lit.)
Molecular Formula	C₁₅H₁₁NO
Molecular Weight	221.25400
Flash Point	237.5ºC
Exact Mass	221.08400
PSA	32.86000
LogP	3.64740
Vapour Pressure	9.47E-09mmHg at 25°C
Index of Refraction	1.709
InChIKey	IFIFXODAHZPTEY-UHFFFAOYSA-N
SMILES	O=Cc1c(-c2ccccc2)[nH]c2ccccc12

Safety Information

Symbol	GHS07
Signal Word	Warning
Hazard Statements	H315-H319-H335
Precautionary Statements	P261-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes	Xi: Irritant;
Risk Phrases	R36/37/38
Safety Phrases	S26-S36
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%

Articles4

Synthesis of 2-arylindole derivatives and evaluation as nitric oxide synthase and NFκB inhibitors.

Org. Biomol. Chem. 10(44) , 8835-47, (2012)

Development of small molecule drug-like inhibitors blocking both nitric oxide synthase and NFκB could offer a synergistic therapeutic approach in the prevention and treatment of inflammation and cance...

Iridium-catalyzed regio- and enantioselective N-allylation of indoles.

Angew. Chem. Int. Ed. Engl. 48(42) , 7841-4, (2009)

Novel indium-mediated ternary reactions between indole-3-carboxaldehydes-allyl bromide-enamines: facile synthesis of bisindolyl-and indolyl-heterocyclic alkanes. Kumar S, et al.

Tetrahedron Lett. 44(10) , 2101-2104, (2003)

Synonyms

MFCD00435481

2-Phenylindole-3-carbaldehyde

2-phenyl-3-formylindole

3-Formyl-2-phenylindole

2-phenyl-1H-indol-3-carboxaldehyde

2-Phenylindole-3-carboxaldehyde

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