2-Cyanobenzaldehyde

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
284.9±23.0 °C at 760 mmHg

[ Melting Point ]:
103-105 °C(lit.)

[ Molecular Formula ]:
C₈H₅NO

[ Molecular Weight ]:
131.131

[ Flash Point ]:
126.1±22.6 °C

[ Exact Mass ]:
131.037109

[ PSA ]:
40.86000

[ LogP ]:
1.45

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.552

Click to get detail MSDS

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H312-H315-H319-H332-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

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

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S26-S37/39-S36/37/39

[ RIDADR ]:
UN 3439 6.1/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2926909090

Click to get detail synthetic route

Precursor

DownStream

[ HS Code ]: 2926909090

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Diastereoselective one-pot tandem synthesis of 3-substituted isoindolinones: a mechanistic investigation.

J. Org. Chem. 75(17) , 5882-7, (2010)

The mechanism of a base-catalyzed one-pot reaction of 2-cyanobenzaldehyde and primary nitroalkanes, to produce 3-substituted isoindolinones, has been investigated. A route starting with a nitroaldol (...

Bifunctional phase-transfer catalysis in the asymmetric synthesis of biologically active isoindolinones.

Beilstein J. Org. Chem. 11 , 2591-9, (2015)

New bifunctional chiral ammonium salts were investigated in an asymmetric cascade synthesis of a key building block for a variety of biologically relevant isoindolinones. With this chiral compound in ...

The aldol addition of readily enolizable 1, 3-dicarbonyl compounds to 2-cyanobenzaldehyde in the synthesis of novel 3-substituted isoindolinones. More V, et al.

Synthesis 2011(18) , 3027-31, (2011)

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