chloropyrimidine structure
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Common Name | chloropyrimidine | ||
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CAS Number | 1722-12-9 | Molecular Weight | 114.533 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 199.2±0.0 °C at 760 mmHg | |
Molecular Formula | C4H3ClN2 | Melting Point | 63-66 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 109.2±4.3 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 2-Chloropyrimidine |
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Synonym | More Synonyms |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 199.2±0.0 °C at 760 mmHg |
Melting Point | 63-66 °C(lit.) |
Molecular Formula | C4H3ClN2 |
Molecular Weight | 114.533 |
Flash Point | 109.2±4.3 °C |
Exact Mass | 113.998474 |
PSA | 25.78000 |
LogP | 0.36 |
Vapour Pressure | 0.5±0.3 mmHg at 25°C |
Index of Refraction | 1.535 |
Storage condition | Refrigerator |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H319 |
Precautionary Statements | P301 + P312 + P330-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xi:Irritant |
Risk Phrases | R36/38 |
Safety Phrases | S26-S37/39 |
RIDADR | 2811 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 6.1(b) |
HS Code | 2933599090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2933599090 |
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Summary | 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Cobalt-catalyzed cross-coupling between in situ prepared arylzinc halides and 2-chloropyrimidine or 2-chloropyrazine.
J. Org. Chem. 74(8) , 3221-4, (2009) A cobalt-catalyzed cross-coupling of aryl halides with 2-chloropyrimidines or 2-chloropyrazines is reported in satisfactory to high yields. The key step of this procedure is the formation of aromatic ... |
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Ru-catalysed C-H arylation of indoles and pyrroles with boronic acids: scope and mechanistic studies.
Chemistry 21(14) , 5380-6, (2015) The Ru-catalysed C2-H arylation of indoles and pyrroles by using boronic acids under oxidative conditions is reported. This reaction can be applied to tryptophan derivatives and tolerates a wide range... |
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Expedient parallel synthesis of 2-amino-4-heteroarylpyrimidines.
Org. Lett. 7(19) , 4113-6, (2005) [reaction: see text] An expedient synthesis of diverse 2-amino-4-heteroarylpyrimidines via a 2-chloropyrimidine intermediate is described. A series of potentially biologically active analogues have be... |
2-Chloro-4-deoxyuracil |
2-Chloro-pyrimindine |
EINECS 217-020-2 |
chloro-pyrimidine |
2-Chloropyrimindine |
MFCD00006060 |
chloropyrimidine |
2-pyrimidyl chloride |
2-Chloropyrimidine |
2-Cl-pyrimidine |
Pyrimidine, 2-chloro- |
2CPY X HCL |
2-Chloro |
pyrimidin-2-yl chloride |
2-chloro-pyrimidine |
2-chloro-pyrimidin |
2-choropyrimidine |
PYRIMIDINE,2-CHLORO |
2-pyrimidinyl chloride |
2-chloropyrimide |