trans-Cinnamonitrile structure
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Common Name | trans-Cinnamonitrile | ||
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CAS Number | 1885-38-7 | Molecular Weight | 129.159 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 263.8±0.0 °C at 760 mmHg | |
Molecular Formula | C9H7N | Melting Point | 18-20 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 105.2±11.2 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | Cinnamonitrile |
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Synonym | More Synonyms |
Density | 1.0±0.1 g/cm3 |
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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 |
Symbol |
GHS07 |
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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 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2926909090 |
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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% |
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)... |
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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... |
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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... |
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 |