3-Aminopyridine structure
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Common Name | 3-Aminopyridine | ||
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CAS Number | 462-08-8 | Molecular Weight | 94.115 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 251.0±0.0 °C at 760 mmHg | |
Molecular Formula | C5H6N2 | Melting Point | 60-63 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 126.0±7.0 °C | |
Symbol |
GHS06, GHS08 |
Signal Word | Danger |
Name | 3-Aminopyridine |
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Synonym | More Synonyms |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 251.0±0.0 °C at 760 mmHg |
Melting Point | 60-63 °C(lit.) |
Molecular Formula | C5H6N2 |
Molecular Weight | 94.115 |
Flash Point | 126.0±7.0 °C |
Exact Mass | 94.053101 |
PSA | 38.91000 |
LogP | -0.02 |
Vapour Pressure | 0.0±0.5 mmHg at 25°C |
Index of Refraction | 1.588 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS06, GHS08 |
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Signal Word | Danger |
Hazard Statements | H301-H311-H315-H319-H331-H335-H373 |
Precautionary Statements | P261-P280-P301 + P310-P305 + P351 + P338-P311 |
Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges |
Hazard Codes | T:Toxic |
Risk Phrases | R25;R36/37/38 |
Safety Phrases | S36/37/39-S45-S37/39-S28B-S26 |
RIDADR | UN 2671 6.1/PG 2 |
WGK Germany | 3 |
RTECS | US1650000 |
Packaging Group | II |
Hazard Class | 6.1 |
HS Code | 2933399090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2933399090 |
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Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Anharmonic vibrational analysis of 3,4-diaminopyridine and 3-aminopyridine by density functional theory calculations.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 76(5) , 502-12, (2010) In this work, we will report a combined experimental and theoretical study on molecular structure and vibrational analysis of 3,4-diaminopyridine (3,4-DAP) and 3-aminopyridine (3-AP). The Fourier tran... |
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Evaluation of electrophilic heteroaromatic substitution: synthesis of heteroaromatic-fused pyrimidine derivatives via sequential three-component heterocyclization.
J. Org. Chem. 77(19) , 8492-500, (2012) A new sequential three-component heterocyclization was developed by reacting aromatic and heterocyclic substrates, including aminobenzenes, 1-aminonaphthalene, 2-aminopyrazines, 5-aminopyrazoles, 3-am... |
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The significance of the temporal bond polarizabilty relaxation of 2- and 3-aminopyridine by 514.5 nm excitation for the nonresonant Raman virtual states.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 71(4) , 1588-93, (2008) Our algorithm [B. Tian, G. Wu, G. Liu, J. Chem. Phys. 87 (1987) 7300] is introduced to obtain the temporal bond polarizabilities of 2- and 3-aminopyridine from their Raman intensities, which supply fr... |
B-PYRIDYLAMINE |
5-amino pyridine |
pyridin-3-ylamine |
3-amino-pyridin |
T6NJ CZ |
pyridine-3-amine |
3APY |
3-amino-pyridine |
3-Aminopyridine |
m-Aminopyridine |
3-pyridinylamine |
3-Pyridinamine |
pyridin-3-amine |
EINECS 207-322-2 |
3-PYRIDYLAMINE |
3-aminepyridin |
MFCD00006400 |