Pivaldehyde structure
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Common Name | Pivaldehyde | ||
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CAS Number | 630-19-3 | Molecular Weight | 86.132 | |
Density | 0.8±0.1 g/cm3 | Boiling Point | 77.5±0.0 °C at 760 mmHg | |
Molecular Formula | C5H10O | Melting Point | 6 °C(lit.) | |
MSDS | Chinese USA | Flash Point | -13.2±7.8 °C | |
Symbol |
GHS02, GHS07 |
Signal Word | Danger |
Name | Trimethylacetaldehyde |
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Synonym | More Synonyms |
Density | 0.8±0.1 g/cm3 |
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Boiling Point | 77.5±0.0 °C at 760 mmHg |
Melting Point | 6 °C(lit.) |
Molecular Formula | C5H10O |
Molecular Weight | 86.132 |
Flash Point | -13.2±7.8 °C |
Exact Mass | 86.073166 |
PSA | 17.07000 |
LogP | 1.07 |
Vapour Pressure | 96.5±0.1 mmHg at 25°C |
Index of Refraction | 1.384 |
Storage condition | 2-8°C |
Water Solubility | Negligible |
Symbol |
GHS02, GHS07 |
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Signal Word | Danger |
Hazard Statements | H225-H315-H335 |
Precautionary Statements | P210-P261 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | F:Flammable |
Risk Phrases | R11 |
Safety Phrases | S16-S23 |
RIDADR | UN 1989 3/PG 2 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 3 |
HS Code | 2912190090 |
Precursor 8 | |
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DownStream 8 | |
HS Code | 2912190090 |
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Summary | 2912190090 acyclic aldehydes without other oxygen function。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0% |
Tetrahedron Asymmetry 17 , 2659, (2006)
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Double stereodifferentiation in the catalytic asymmetric aziridination of imines prepared from α-chiral amines.
Chemistry 18(17) , 5302-13, (2012) The catalytic asymmetric aziridination of imines and diazo compounds (AZ reaction) mediated by boroxinate catalysts derived from the VANOL and VAPOL ligands was investigated with chiral imines derived... |
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Diastereomeric Reissert compounds of isoquinoline and 6,7-dimethoxy-3,4-dihydroisoquinoline in stereoselective synthesis.
J. Org. Chem. 72(15) , 5759-70, (2007) Chiral acid chlorides were reacted with isoquinoline and 6,7-dimethoxy-3,4-dihydroisoquinoline to form diastereomeric Reissert compounds 8-11 and 18-21, respectively. The best diastereoselectivity (80... |
2,2-Dimethylpropanal |
α,α-Dimethylpropanal |
Pivalaldehyde |
Propanal, 2,2-dimethyl- |
trimethylacetaldehyde |
2,2-Dimethylpropionaldehyde |
Pivalic aldehyde |
EINECS 211-134-6 |
MFCD00006962 |
α,α-Dimethylpropionaldehyde |