(S)-(+)-Benzyl glycidyl ether structure
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Common Name | (S)-(+)-Benzyl glycidyl ether | ||
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CAS Number | 16495-13-9 | Molecular Weight | 164.201 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 252.7±15.0 °C at 760 mmHg | |
Molecular Formula | C10H12O2 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 100.9±19.9 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | (S)-(+)-Benzyl glycidyl ether |
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Synonym | More Synonyms |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 252.7±15.0 °C at 760 mmHg |
Molecular Formula | C10H12O2 |
Molecular Weight | 164.201 |
Flash Point | 100.9±19.9 °C |
Exact Mass | 164.083725 |
PSA | 21.76000 |
LogP | 2.04 |
Vapour Pressure | 0.0±0.5 mmHg at 25°C |
Index of Refraction | 1.535 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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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-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | TX2860030 |
HS Code | 2910900090 |
HS Code | 2910900090 |
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Summary | 2910900090. epoxides, epoxyalcohols, epoxyphenols and epoxyethers, with a three-membered ring, and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
Bioresolution of benzyl glycidyl ether using whole cells of Bacillus alcalophilus.
J. Basic Microbiol. 52(4) , 383-9, (2012) The incubation of whole Bacillus alcalophilus cells grown on a mineral supplemented medium (MSM) containing 1% (w/v) sucrose as carbon source, 1.2% (w/v) tryptone as nitrogen source at pH 6.5 and temp... |
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Metal-mediated cyclization of aryl and benzyl glycidyl ethers: a complete scenario.
J. Am. Chem. Soc. 130(50) , 16838-9, (2008) Enantiomerically pure aryl and benzyl glycidyl ethers undergo stereospecific cyclizations leading to 3-chromanols or to tetrahydrobenzo[c]oxepin-4-ols under mild conditions in the presence of a cataly... |
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Enantioselective total synthesis of (+)-gigantecin: exploiting the asymmetric glycolate aldol reaction.
J. Am. Chem. Soc. 126(40) , 12790-1, (2004) The enantioselective synthesis of the potent, selective, cytotoxic, annonaceous acetogenin, (+)-gigantecin, has been completed. An asymmetric glycolate aldol serves to establish the stereocenters at C... |
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