trans-Cinnamonitrile

Names

[ Name ]:
trans-Cinnamonitrile

[Synonym ]:
Cinnamonitrile
3-phenylacrylonitrile
EINECS 217-552-5
(E)-3-Phenylacrylonitrile
2-Propenenitrile, 3-phenyl-, (E)-
trans-cinnamonitrile
trans-3-Phenyl-2-propenenitrile
CINNAMALVA
(2E)-3-phenylprop-2-enenitrile
trans-β-Phenylacrylonitrile
cyanostyrene
CINNAMYL NITRILE
(2E)-3-Phenylacrylonitrile
Cinnamonitrile, (E)-
STYRYL CYANIDE
naMonitrile
Cinnamonitril
2-Propenenitrile, 3-phenyl-, (2E)-
MFCD00001930
trans-3-Phenylpropenonitrile
Ciamonitrile
(E)-Cinnamonitrile
β-Cyanostyrene

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
263.8±0.0 °C at 760 mmHg

[ Melting Point ]:
18-20 °C(lit.)

[ Molecular Formula ]:
C₉H₇N

[ Molecular Weight ]:
129.159

[ Flash Point ]:
105.2±11.2 °C

[ Exact Mass ]:
129.057846

[ PSA ]:
23.79000

[ LogP ]:
2.32

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.595

[ Water Solubility ]:
insoluble

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
3276

[ WGK Germany ]:
3

[ RTECS ]:
UD1440000

[ Packaging Group ]:
I; II; III

[ Hazard Class ]:
6.1

[ HS Code ]:
2926909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ 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%

Articles

The spectroscopy and photochemistry of quinioline structural isomers: (E)- and (Z)-phenylvinylnitrile.

J. Chem. Phys. 143 , 074304, (2015)

In Titan's atmosphere, photochemical pathways that lead to nitrogen heteroaromatics may incorporate photoisomerization of their structural isomers as a final step. (E)- and (Z)-phenylvinylnitrile ((E)...

Reversible targeting of noncatalytic cysteines with chemically tuned electrophiles.

Nat. Chem. Biol. 8 , 471-6, (2012)

Targeting noncatalytic cysteine residues with irreversible acrylamide-based inhibitors is a powerful approach for enhancing pharmacological potency and selectivity. Nevertheless, concerns about off-ta...

Formation of mercapturic acids from acrylonitrile, crotononitrile, and cinnamonitrile by direct conjugation and via an intermediate oxidation process.

Drug Metab. Dispos. 9(3) , 246-9, (1981)

After administration of acrylonitrile, crotononitrile and cinnamonitrile to rats, two types of mercapturic acids were isolated from urine and identified by mass and NMR spectroscopy as N-acetyl-S-(2-c...