2-AMINO-1-BIPHENYL-4-YL-ETHANONE HYDROCHLORIDE

Base Information

• Chemical Name: 2-AMINO-1-BIPHENYL-4-YL-ETHANONE HYDROCHLORIDE
• CAS No.: 71350-68-0
• Molecular Formula: C14H14ClNO
• Molecular Weight: 247.72
• Hs Code.: 2922399090
• Mol file: 71350-68-0.mol

Synonyms:2-AMINO-1-BIPHENYL-4-YL-ETHANONE HYDROCHLORIDE;2-AMINO-1-(1,1'-BIPHENYL-4-YL)ETHANONE HYDROCHLORIDE

Chemical Property of 2-AMINO-1-BIPHENYL-4-YL-ETHANONE HYDROCHLORIDE

Chemical Property:

• PSA: 43.09000
• LogP: 3.99730

Purity/Quality:

98%min ^*data from raw suppliers

2-Amino-1-biphenyl-4-ylethanone hydrochloride 95%+ ^*data from reagent suppliers

Safty Information:

• Statements: 36
• Safety Statements: 26

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2-AMINO-1-BIPHENYL-4-YL-ETHANONE HYDROCHLORIDE

There total 6 articles about 2-AMINO-1-BIPHENYL-4-YL-ETHANONE 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: 99.0%

C16H13NO3 (127118-90-5) → 2-Amino-1-biphenyl-4-yl-ethanone; hydrochloride (71350-68-0)

Guidance literature:

With hydrogenchloride; at 120 ℃; for 0.5h;

DOI:10.1055/s-1990-26959

Reference yield:

2-Bromo-4'-phenylacetophenone (135-73-9) → 2-Amino-1-biphenyl-4-yl-ethanone; hydrochloride (71350-68-0)

Guidance literature:

With chloroform; hexamethylenetetramine; Behandeln des Reaktionsprodukts mit wss.-aethanol. Salzsaeure;

DOI:10.1021/jo01189a015

Reference yield:

(4-phenyl-phenacyl)-hexamethylenetetraminium; bromide (5520-63-8) → 2-Amino-1-biphenyl-4-yl-ethanone; hydrochloride (71350-68-0) + 2-[1,1'-biphenyl]-4-yl-2-oxoethylammonium bromide

Guidance literature:

With hydrogenchloride; In ethanol; for 72h; Title compound not separated from byproducts; Ambient temperature;

DOI:10.1135/cccc19932720

upstream raw materials:

1-(biphenyl-4-yl)ethanamine

2-Bromo-4'-phenylacetophenone

C₁₆H₁₃NO₃

(4-phenyl-phenacyl)-hexamethylenetetraminium; bromide

Downstream raw materials:

N-(4-phenyl-phenacyl)-[1]naphthamide

4-(5-biphenyl-4-yl-oxazol-2-yl)-naphthalene-1,8-dicarboxylic acid anhydride

5-([1,1'-biphenyl]-4-yl)oxazole

2'-(5-Biphenyl-4-yl-oxazol-2-yl)-biphenyl-2-carboxylic acid