1H-Indole-3-carboxaldehyde,1-(phenylmethyl)-

Names

[ Name ]:
1H-Indole-3-carboxaldehyde,1-(phenylmethyl)-

[Synonym ]:
1-Benzyl-1H-indole-3-carboxaldehyde
1-benzyl-1H-indole-3-carbaldehyde
N-benzylindole-3-carboxaldehyde
1-Benzyl-3-indolylaldehyde
1-benzyl-3-indole carboxaldehyde
1-benzylindol-3-carboxaldehyde
1-Benzylindole-3-carboxaldehyde
MFCD00022894

Chemical & Physical Properties

[ Density]:
1.1g/cm3

[ Boiling Point ]:
439.8ºC at 760mmHg

[ Melting Point ]:
107ºC

[ Molecular Formula ]:
C₁₆H₁₃NO

[ Molecular Weight ]:
235.28100

[ Flash Point ]:
219.8ºC

[ Exact Mass ]:
235.10000

[ PSA ]:
22.00000

[ LogP ]:
3.50210

[ Vapour Pressure ]:
6.19E-08mmHg at 25°C

[ Index of Refraction ]:
1.606

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H317

[ Precautionary Statements ]:
P280

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Faceshields;Gloves

[ Hazard Codes ]:
Xn,C,Xi

[ Risk Phrases ]:
R22

[ Safety Phrases ]:
36/37

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

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

Analogues and derivatives of oncrasin-1, a novel inhibitor of the C-terminal domain of RNA polymerase II and their antitumor activities.

Med. Chem. 54 , 2668, (2011)

To optimize the antitumor activity of oncrasin-1, a small molecule RNA polymerase II inhibitor, we evaluated 69 oncrasin-1 analogues for their cytotoxic activity against normal human epithelial cells ...

Discovery and development of thiazolo[3,2-a]pyrimidinone derivatives as general inhibitors of Bcl-2 family proteins.

ChemMedChem 6 , 904, (2011)

A class of compounds with a common thiazolo[3,2-a]pyrimidinone motif has been developed as general inhibitors of Bcl-2 family proteins. The lead compound was originally identified in a random screenin...

Application of Nazarov type electrocyclization to access [6,5,6] and [6,5,5] core embedded new polycycles: an easy entry to tetrahydrofluorene scaffolds related to Taiwaniaquinoids and C-nor-D homosteroids.

Org. Biomol. Chem. 9 , 4782, (2011)

An easy, efficient and concise approach to tetrahydrofluorene [6,5,6]ABC tricyclic core embedded new polycycles has been achieved under relatively mild and catalytic Nazarov type electrocyclization co...