2-((Benzyloxy)methyl)oxirane structure
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Common Name | 2-((Benzyloxy)methyl)oxirane | ||
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CAS Number | 2930-05-4 | 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 | 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 |
Storage condition | Refrigerator |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATAMUTATION 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 |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S37-S39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | TX2860000 |
HS Code | 2910900090 |
Precursor 9 | |
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DownStream 10 | |
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% |
Synthesis of atactic and isotactic poly(1,2-glycerol carbonate)s: degradable polymers for biomedical and pharmaceutical applications.
J. Am. Chem. Soc. 135(18) , 6806-9, (2013) The synthesis and characterization of atactic and isotactic linear poly(benzyl 1,2-glycerol carbonate)s are reported. The poly(benzyl 1,2-glycerol carbonate)s were obtained via the ring-opening copoly... |
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Biocatalytic resolution of benzyl glycidyl ether and its derivates by Talaromyces flavus: effect of phenyl ring substituents on enantioselectivity.
Biotechnol. Lett. 34(8) , 1499-503, (2012) Talaromyces flavus containing a constitutive epoxide hydrolase (EH) resolved racemic benzyl glycidyl ether and nine derivatives into their (R)-enantiomers. After optimization of the fermentation condi... |
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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... |
2-[(Benzyloxy)methyl]oxirane |
MFCD00068664 |
(+)-(Benzyloxymethyl)oxirane |
Oxirane, [(phenylmethoxy)methyl]- |
3-benzyloxypropyleneoxide |
1-Benzyloxy-2,3-epoxypropane |
(+)-Benzyl glycidyl ether |
(R)-Benzyl glycidyl ether |
(S)-Benzyl glycidyl ether |
3-benzyloxy-1,2-epoxypropane |
rac-benzyl glycidyl ether |
2-((Benzyloxy)methyl)oxirane |
rac-taxifolin |
EINECS 220-899-5 |
Oxirane, 2-[(phenylmethoxy)methyl]- |
2-(Benzyloxymethyl)oxirane |
rac-1'-acetoxydihydrochavicol acetate |
phenylmethoxymethyloxirane |
rac-dihydrogalangal acetate |
Dihydrogalangal acetate |