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

Modify Date: 2024-01-11 19:20:02

1H-Indole-3-carboxaldehyde,1-(phenylmethyl)- Structure
1H-Indole-3-carboxaldehyde,1-(phenylmethyl)- structure
Common Name 1H-Indole-3-carboxaldehyde,1-(phenylmethyl)-
CAS Number 10511-51-0 Molecular Weight 235.28100
Density 1.1g/cm3 Boiling Point 439.8ºC at 760mmHg
Molecular Formula C16H13NO Melting Point 107ºC
MSDS Chinese USA Flash Point 219.8ºC
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name 1-benzylindole-3-carbaldehyde
Synonym More Synonyms

 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

 Safety Information

Symbol GHS07
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%

 Articles4

More 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...

 Synonyms

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