Grundinformationen
- Standard-SMILES
Cc1ccc2nc(Cl)[nH]c2c1- InChIKey
KBSHNSLMNALPCU-UHFFFAOYSA-N- Summenformel
- C8H7ClN2
- Durchschnittliche Molmasse
- 166,61 g/mol
- Monoisotopische Masse
- 166,0297759
Namen und Bezeichner
- Bevorzugter Name
- 2-chloro-6-methyl-1H-1,3-benzodiazole
- IUPAC
- 2-chloro-6-methyl-1H-benzimidazole
- Englischer Name
- 1H-Benzimidazole,2-chloro-5-methyl-(9CI)
- Summenformel
- C8H7ClN2
- Molmasse
- 166.61
Namen und Synonyme
2-chloro-6-methyl-1H-1,3-benzodiazoleRefChem:469681841-058-44887-94-92-Chloro-5-methyl-1H-benzo[d]imidazole2-chloro-5-methylbenzimidazole2-chloro-6-methyl-1H-benzimidazole2-chloro-5-methyl-1H-benzimidazole1H-Benzimidazole,2-chloro-5-methyl-(9CI)MFCD110466722-CHLORO-5-METHYL-1H-1,3-BENZODIAZOLE1H-benzimidazole, 2-chloro-5-methyl-, hydrochloride
Weitere Namen anzeigen
2-chloro-5-methyl-1H-benzimidazole()1H-Benzimidazole, 2-chloro-6-methyl-2-chloro-6-methyl-1H-benzo[d]imidazole
2-chloro-6-methyl-1H-benzoimidazoleSCHEMBL827359SCHEMBL3490546SCHEMBL28246494DTXSID70469680KBSHNSLMNALPCU-UHFFFAOYSA-NALBB-016175XH0011
Datenbank-Bezeichner
- CAS
4887-94-9- PubChem CID
- 11629655
- DTXSID
DTXSID70469680- EC Number
- 841-058-4
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 2,4
- Polarare Oberfläche (TPSA)
- 28,7 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 1
- Frei drehbare Bindungen
- 0
- Schwere Atome
- 11
- Formalladung
- 0
- Komplexität
- 151
Physikochemische Eigenschaften
- Schmelzpunkt
- 176 · 176-180 °C
- Siedepunkt
- 339.9 · 339.9±35.0 °C(Predicted)
- Dichte
- 1.351 · 1.351±0.06 g/cm3(Predicted)
- storage temp.
- 2 · under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 9.84 · 9.84±0.10(Predicted)
- Aggregatzustand
- solid
- InChI
- 1S/C8H7ClN2/c1-5-2-3-6-7(4-5)11-8(9)10-6/h2-4H,1H3,(H,10,11)
- InChIKey
- KBSHNSLMNALPCU-UHFFFAOYSA-N
Sicherheit und Regulatorisches
Sicherheitsdaten
- wgk
- WGK 3
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Aquatic Acute 1Aquatic Chronic 1Eye Irrit. 2Skin Irrit. 2Skin Sens. 1
Chemie und Industrie
Anwendungen
Verwenden2-Chloro-5-methylbenzimidazole acts as a reagent for the design and synthesis of prostate cancer antigen-1 (PCA-1/ALKBH3) inhibitors as anti-prostate cancer drug, synthesis of unsymmetrical 2,2’-bisbenzimidazole sulfide of pharmacological interest.
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