4-Chloro-3-fluorobenzylamine hydrochloride

Base Information

• Chemical Name: 4-Chloro-3-fluorobenzylamine hydrochloride
• CAS No.: 202982-64-7
• Molecular Formula: C7H8Cl2FN
• Molecular Weight: 196.052
• Hs Code.: 2921490090
• European Community (EC) Number: 871-701-4
• Mol file: 202982-64-7.mol

Synonyms:4-Chloro-3-fluorobenzylamine hydrochloride;202982-64-7;(4-chloro-3-fluorophenyl)methanamine hydrochloride;(4-chloro-3-fluorophenyl)methanamine;hydrochloride;SCHEMBL5958057;SZEIBCAEFIKNJV-UHFFFAOYSA-N;MFCD00143293;4-CHLORO-3-FLUOROBENZYLAMINE HCL;CS-0436377;N12136;(4-chloro-3-fluorophenyl)methanaminehydrochloride;EN300-2009729;Z3244773428

Chemical Property of 4-Chloro-3-fluorobenzylamine hydrochloride

Chemical Property:

• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 195.0017828
• Heavy Atom Count: 11
• Complexity: 110

Purity/Quality:

97% ^*data from raw suppliers

4-CHLORO-3-FLUOROBENZYLAMINE HYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Hazard Codes: C

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1CN)F)Cl.Cl

Technology Process of 4-Chloro-3-fluorobenzylamine hydrochloride

There total 1 articles about 4-Chloro-3-fluorobenzylamine hydrochloride 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:

→ 4-chloro-3-fluoro-benzylamine hydrochloride (202982-64-7)

Guidance literature:

Reference yield: 46.0%

4-chloro-3-fluoro-benzylamine hydrochloride (202982-64-7) + Ethyl oxalyl chloride (4755-77-5) → ethyl 2-[(4-chloro-3-fluorophenyl)methylamino]-2-oxoacetate

Guidance literature:

With triethylamine; In dichloromethane; for 1h;

DOI:10.1016/j.ejmech.2021.113681

Refernces