4-Chloro-1H-imidazo[4,5-c]pyridine

HCID 5373364CAS 2770-01-6

Completing data — usually done within a minute

Substructure search Find similar structures

Basic information

Standard SMILES: Clc1nccc2[nH]cnc12
InChIKey: DHJMLXBBZRWBPW-UHFFFAOYSA-N
Molecular formula: C6H4ClN3
Average molar mass: 153.572 g/mol
Monoisotopic mass: 153.00937481

Names & identifiers

Preferred name: 4-Chloro-1H-imidazo[4,5-c]pyridine
IUPAC: 4-Chloro-1H-imidazo[4,5-c]pyridine
English name: 4-Chloro-1-H-imidazo[4,5-c]pyridine
Molecular formula: C6H4ClN3
Molecular weight: 153.57

Names & synonyms

4-CHLORO-1-H-IMIDAZO[44-Chloro-1-H-imidazo[4,5-c]pyridine3H-IMidazo[4,5-c]pyridine, 4-chloro-4-Chloro-1H-imidazo[4,5-c]pyridine 98%4-CHLORO-1-H-IMIDAZO[4,5-C]PYRIDINE ISO 9001：2015 REACH4-CHLORO-1-H-IMIDAZO[4,5-C]PYRIDINE4-CHLORO-1-H-IMIDAZO[4,5-C]PYRIDINE

Database identifiers

CAS: 2770-01-6
PubChem CID: 5373364
DTXSID: DTXSID90418716
ChEMBL: CHEMBL33524
EC Number: 810-345-6
Nikkaji: J2.339.778A

Properties

Physicochemical properties

Melting point: 179 · 179-181 °C
Boiling point: 455.4 · 455.4±25.0 °C(Predicted)
Density: 1.531 · 1.531±0.06 g/cm3(Predicted)
storage temp.: 2 · under inert gas (nitrogen or Argon) at 2-8°C
solubility: DMSO (Slightly, Sonicated), Methanol (Slightly, Sonicated)
form: Solid
pka: 7.93 · 7.93±0.40(Predicted)
color: Pale Beige to Pale Brown
InChI: InChI=1S/C6H4ClN3/c7-6-5-4(1-2-8-6)9-3-10-5/h1-3H,(H,9,10)
InChIKey: DHJMLXBBZRWBPW-UHFFFAOYSA-N
SMILES: C1(Cl)=NC=CC2N=CNC1=2
Symbol(GHS): 7 · GHS07
Signal word: Warning
Hazard statements: 302 · H302-H315-H319-H335
Precautionary statements: 261 · P261-P305+P351+P338
HS Code: 2933399990 · 2933399990

Safety & regulation

Safety data

hs_code: 2933399990
Signal word: Warning
Symbol(GHS): GHS07
Hazard statements: H302-H315-H319-H335
Precautionary statements: P261-P305+P351+P338

Chemistry & industry

Applications

Uses4-Chloro-1H-imidazo[4,5-c]pyridine is used as a reagent in the synthesis of 3-bromo-3-deazaneplanocin and 3-bromo-3-deazaaristeromycin, compounds which exhibit antiviral activity.