Cinnamyl alcohol structure
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Common Name | Cinnamyl alcohol | ||
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CAS Number | 104-54-1 | Molecular Weight | 134.175 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 250.0±0.0 °C at 760 mmHg | |
Molecular Formula | C9H10O | Melting Point | 30-33 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 124.8±14.5 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of Cinnamyl alcoholCinnamyl Alcohol is an active component from chestnut flower, inhibits increased PPARγ expression, with anti-obesity activity[1]. |
Name | cinnamyl alcohol |
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Synonym | More Synonyms |
Description | Cinnamyl Alcohol is an active component from chestnut flower, inhibits increased PPARγ expression, with anti-obesity activity[1]. |
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Related Catalog | |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 250.0±0.0 °C at 760 mmHg |
Melting Point | 30-33 °C(lit.) |
Molecular Formula | C9H10O |
Molecular Weight | 134.175 |
Flash Point | 124.8±14.5 °C |
Exact Mass | 134.073166 |
PSA | 20.23000 |
LogP | 1.70 |
Vapour density | 4.6 (vs air) |
Vapour Pressure | 0.0±0.5 mmHg at 25°C |
Index of Refraction | 1.599 |
Storage condition | 2-8°C |
Stability | Stable. Incompatible with strong oxidizing agents. |
Water Solubility | 1.8 g/L (20 ºC) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H315-H317-H319 |
Precautionary Statements | P280-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xn:Harmful |
Risk Phrases | R22;R36;R43 |
Safety Phrases | S26-S36/37-S37/39-S24 |
RIDADR | 2811 |
WGK Germany | 2 |
RTECS | GE2200000 |
Hazard Class | 6.1 |
HS Code | 2912299000 |
Precursor 9 | |
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DownStream 9 | |
HS Code | 2912299000 |
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Summary | 2912299000. other cyclic aldehydes without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
Parallel dual secondary column-dual detection: a further way of enhancing the informative potential of two-dimensional comprehensive gas chromatography.
J. Chromatogr. A. 1360 , 264-74, (2014) Comprehensive two-dimensional gas chromatography (GC×GC) coupled with Mass Spectrometry (MS) is one of today's most powerful analytical platforms for detailed analysis of medium-to-high complexity sam... |
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Functional characterization of two acyltransferases from Populus trichocarpa capable of synthesizing benzyl benzoate and salicyl benzoate, potential intermediates in salicinoid phenolic glycoside biosynthesis.
Phytochemistry 113 , 149-59, (2015) Salicinoids are phenolic glycosides (PGs) characteristic of the Salicaceae and are known defenses against insect herbivory. Common examples are salicin, salicortin, tremuloidin, and tremulacin, which ... |
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Contribution of cinnamic acid analogues in rosmarinic acid to inhibition of snake venom induced hemorrhage.
Bioorg. Med. Chem. 19 , 2392-6, (2011) In our previous paper, we reported that rosmarinic acid (1) of Argusia argentea could neutralize snake venom induced hemorrhagic action. Rosmarinic acid (1) consists of two phenylpropanoids: caffeic a... |
cinnamic alcohol |
stylone |
trans-3-phenyl-2-propen-1-ol |
Peruvin |
Ciamyl alcohol |
STYRYL CARBINOL |
Cinnamylalkohol |
(E)-cinnamyl alcohol |
(E)-3-phenylprop-2-en-1-ol |
3-PHENYLALLYLOL |
EINECS 203-212-3 |
(2E)-3-phenylprop-2-en-1-ol |
Sterone |
MFCD00002921 |
(2E)-3-Phenyl-2-propen-1-ol |
Cinnamyl alcohol |
3-phenylprop-2-en-1-ol |
3-Phenyl |
allylic benzylic alcohol |
cinnamyl alcohol, (E)-isomer |
Chnnamyl alcohol |
cynnamyl alcohol |
Styrylicalcohol |
3-phenyl-2-propen-1-ol |
2-Propen-1-ol, 3-phenyl-, (2E)- |