trans-Cinnamonitrile
Names
[ CAS No. ]:
1885-38-7
[ 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
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
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
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...