<Suppliers Price>

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

Names

[ CAS No. ]:
10511-51-0

[ 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

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

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...


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.