2-Acetonaphthone structure
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Common Name | 2-Acetonaphthone | ||
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CAS Number | 93-08-3 | Molecular Weight | 170.207 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 303.0±11.0 °C at 760 mmHg | |
Molecular Formula | C12H10O | Melting Point | 52-56 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 129.5±14.2 °C | |
Symbol |
GHS07, GHS09 |
Signal Word | Warning |
Use of 2-Acetonaphthone2-Acetonaphthone is an endogenous metabolite. |
Name | 2-acetylnaphthalene |
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Synonym | More Synonyms |
Description | 2-Acetonaphthone is an endogenous metabolite. |
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Related Catalog |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 303.0±11.0 °C at 760 mmHg |
Melting Point | 52-56 °C(lit.) |
Molecular Formula | C12H10O |
Molecular Weight | 170.207 |
Flash Point | 129.5±14.2 °C |
Exact Mass | 170.073166 |
PSA | 17.07000 |
LogP | 2.90 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.615 |
Water Solubility | insoluble |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07, GHS09 |
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Signal Word | Warning |
Hazard Statements | H302-H315-H319-H335-H411 |
Precautionary Statements | P261-P273-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn:Harmful; |
Risk Phrases | R22;R36/37/38;R51/53 |
Safety Phrases | S26-S36-S61-S24/25-S22-S36/37 |
RIDADR | UN3077 |
WGK Germany | 3 |
RTECS | DB7084000 |
Packaging Group | III |
Hazard Class | 9 |
HS Code | 29143900 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2914399090 |
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Summary | 2914399090. other aromatic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
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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Organoleptic Characteristics of Flavor Materials Mosciano, G.
Perfum. Flavor. 4th ed., 28 , 104, (2003)
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Mechanisms of Photoreactions in Solution. VI. 1 Reduction of 1-Naphthaldehyde and 2-Acetonaphthone. Hammond GS and Leermakers PA.
J. Am. Chem. Soc. 84(2) , 207-211, (1962)
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1-(2-Naphthyl)ethanone |
ORANGE II |
EINECS 202-216-2 |
MANDARIN G |
ORANGE P |
2-Acetylnaphthalene |
ORANGE 2 |
ORANGER |
1-(naphthalen-2-yl)ethanone |
MFCD00004108 |
ORANGE A |
2-Acetonaphthone |
1-(Naphthalen-2-yl)ethanon |
Ethanone, 1-(2-naphthalenyl)- |
FEMA 2723 |
2'-Acetonaphthone |
1-(2-naphthyl)-ethanone |
β-Acetylnaphthalene |
1-(2-naphthyl)ethan-1-one |
ORANGE Y |
Ethanone, 1- (2-naphthalenyl)- |
CI NO 5510 |
2-acetonaphthalene |
methyl 2-naphthyl ketone |
β-Acetonaphthalene |
METHYL BETA-NAPHTHYL KETON |