5-Chloro-1-ethyl-2-methylbenzimidazole

Base Information

• Chemical Name: 5-Chloro-1-ethyl-2-methylbenzimidazole
• CAS No.: 2818-76-0
• Molecular Formula: C10H11 Cl N2
• Molecular Weight: 194.664
• European Community (EC) Number: 220-576-9
• NSC Number: 97067
• UNII: Z8PP2ATW5R
• DSSTox Substance ID: DTXSID8062652
• Nikkaji Number: J38.296E
• Wikidata: Q72450139
• Mol file: 2818-76-0.mol

Synonyms:5-Chloro-1-ethyl-2-methylbenzimidazole;2818-76-0;1H-Benzimidazole, 5-chloro-1-ethyl-2-methyl-;5-Chloro-1-ethyl-2-methyl-1H-benzo[d]imidazole;5-Chloro-1-ethyl-2-methyl-benzimidazole;Benzimidazole, 5-chloro-1-ethyl-2-methyl-;Z8PP2ATW5R;5-chloro-1-ethyl-2-methyl-1H-benzimidazole;5-chloro-1-ethyl-2-methyl-1H-1,3-benzodiazole;EINECS 220-576-9;NSC 97067;NSC-97067;NSC97067;UNII-Z8PP2ATW5R;Cambridge id 5160785;DTXSID8062652;HMS1681G03;STK396455;AKOS000546995;1-Ethyl-2-methyl-5-chloro-1H-benzimidazole;CS-0333373;5-CHLORO-1-ETHYL-2-METHYLBENZIMIDAZOLE,99%

Chemical Property of 5-Chloro-1-ethyl-2-methylbenzimidazole

Chemical Property:

• Vapor Pressure: 0.000225mmHg at 25°C
• Boiling Point: 336°Cat760mmHg
• Flash Point: 157°C
• Density: 1.22g/cm³
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 194.0610761
• Heavy Atom Count: 13
• Complexity: 186

Purity/Quality:

98%min ^*data from raw suppliers

5-Chloro-1-ethyl-2-methylbenzimidazole ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCN1C(=NC2=C1C=CC(=C2)Cl)C

Technology Process of 5-Chloro-1-ethyl-2-methylbenzimidazole

There total 2 articles about 5-Chloro-1-ethyl-2-methylbenzimidazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

acetic anhydride (108-24-7) + 4-chloro-N1-ethylbenzene-1,2-diamine (62476-15-7) → 5-chloro-1-ethyl-2-methyl-1H-benzoimidazole (2818-76-0)

Guidance literature:

Reference yield:

→ 5-chloro-1-ethyl-2-methyl-1H-benzoimidazole (2818-76-0)

Guidance literature:

Imidazol 24;

upstream raw materials:

acetic anhydride

4-chloro-N¹-ethylbenzene-1,2-diamine