4-Phenylphenyl chloroformate

Base Information

• Chemical Name: 4-Phenylphenyl chloroformate
• CAS No.: 3185-73-7
• Molecular Formula: C13H9ClO2
• Molecular Weight: 232.666
• DSSTox Substance ID: DTXSID50572989
• Wikidata: Q82461542
• Mol file: 3185-73-7.mol

Synonyms:4-phenylphenyl chloroformate;3185-73-7;(4-phenylphenyl) carbonochloridate;[1,1'-Biphenyl]-4-yl carbonochloridate;4-Biphenylyl Chloroformate;4-phenylphenylchloroformate;Biphenyl-4-yl chloroformate;SCHEMBL1347723;DTXSID50572989;ISWLCQXWMQGGOZ-UHFFFAOYSA-N;[1,1'-Biphenyl-4-yl]chloroformate;MFCD24141223;AKOS020226031;SY296913;EN300-281305;G53216

Chemical Property of 4-Phenylphenyl chloroformate

Chemical Property:

• XLogP3: 4.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 232.0291072
• Heavy Atom Count: 16
• Complexity: 228

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CC=C(C=C2)OC(=O)Cl

Technology Process of 4-Phenylphenyl chloroformate

There total 1 articles about 4-Phenylphenyl chloroformate 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-hydroxyphenyl-4'-(4-phenylphenyl)oxycarbonylaminophenyl ether + chlorocarbonic acid biphenyl-4-yl ester (3185-73-7)

Guidance literature:

Reference yield:

6-hydroxy-1,2,3,4-tetrahydro-β-carboline (38421-97-5) + chlorocarbonic acid biphenyl-4-yl ester (3185-73-7) → C24H20N2O3 (1417520-00-3)

Guidance literature:

With triethylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 16h;

DOI:10.1016/j.bmcl.2012.10.137

Reference yield:

chlorocarbonic acid biphenyl-4-yl ester (3185-73-7) + 2-amino-6-bromo-4-methylphenol (343269-51-2) → (3-bromo-2-hydroxy-5-methyl-phenyl)-carbamic acid biphenyl-4-yl ester

Guidance literature:

With diethyl ether; unter Kuehlung;

DOI:10.1021/ja01322a038

Downstream raw materials:

N,N'-hexanediyl-bis-carbamic acid bis-biphenyl-4-yl ester

4-methyl-benzoic acid biphenyl-4-yl ester

biphenyl 4-yl benzoate

C₂₄H₂₀N₂O₃

Refernces