Identification | More | [Name]
2,6-Dichloro-3-nitropyridine | [CAS]
16013-85-7 | [Synonyms]
2,6-DICHLORO-3-NITROPYRIDINE 3-NITRO-2,6-DICHLOROPYRIDINE PYRIDINE, 2,6-DICHLORO-3-NITRO- TIMTEC-BB SBB003614 2,6-DICHLORO-3-NITROPYRIDINE, TECH., 92% DICHLORONITROPYRIDINE 2,6-Dichloro-3-nitro 2,6-DICHLORO-3-NITROPYRIDINE 98+% 2,6-Dichloro-3-nitropyridine ,92% | [EINECS(EC#)]
240-151-1 | [Molecular Formula]
C5H2Cl2N2O2 | [MDL Number]
MFCD00006234 | [Molecular Weight]
192.99 | [MOL File]
16013-85-7.mol |
Chemical Properties | Back Directory | [Appearance]
yellow crystalline powder or chunks | [Melting point ]
55-60 °C(lit.)
| [Boiling point ]
295.5±35.0 °C(Predicted) | [density ]
1.6791 (rough estimate) | [refractive index ]
1.6100 (estimate) | [Fp ]
>230 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
soluble in Methanol | [form ]
Liquid | [pka]
-5.76±0.10(Predicted) | [color ]
Clear colorless to light yellow | [Detection Methods]
GC,NMR | [BRN ]
1619741 | [CAS DataBase Reference]
16013-85-7(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . R42/43:May cause sensitization by inhalation and skin contact . R43:May cause sensitization by skin contact. | [Safety Statements ]
S22:Do not breathe dust . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37:Wear suitable protective clothing and gloves . S37/39:Wear suitable gloves and eye/face protection . S24:Avoid contact with skin . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29333990 |
Hazard Information | Back Directory | [Chemical Properties]
yellow crystalline powder or chunks | [Uses]
2,6-Dichloro-3-nitropyridine was used:
- in the synthesis of pyridyldifluoroacetates
- as starting reagent in the preparation of bicyclooxacalixhetarene
| [General Description]
2,6-Dichloro-3-nitropyridine undergoes macrocyclic condensation reaction with resorcinol derivatives to yield chiral tetraoxacalix[2]arene[2]pyridines. |
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