4'-Isopropyl-4-biphenylol

Base Information

• Chemical Name: 4'-Isopropyl-4-biphenylol
• CAS No.: 22239-54-9
• Molecular Formula: C₁₅H₁₆O
• Molecular Weight: 212.291
• Hs Code.: 2907199090
• European Community (EC) Number: 244-863-3
• DSSTox Substance ID: DTXSID7066772
• Nikkaji Number: J41.824B
• Wikidata: Q81993356
• Mol file: 22239-54-9.mol

Synonyms:4'-ISOPROPYL-4-BIPHENYLOL;22239-54-9;4-Isopropyl-4'-hydroxy biphenyl;p-alpha-Cumylphenol;4-Biphenylol, 4'-isopropyl-;BRN 2519665;EINECS 244-863-3;AI3-14894;(1,1'-Biphenyl)-4-ol, 4'-(1-methylethyl)-;4'-(1-Methylethyl)(1,1'-biphenyl)-4-ol;4'-(1-methylethyl)[1,1'-biphenyl]-4-ol;[1,1'-Biphenyl]-4-ol, 4'-(1-methylethyl)-;4-(p-Cumenyl)phenol;SCHEMBL487609;DTXSID7066772;AKOS002678724;4-hydroxy-4'-(1-methylethyl)biphenyl;LS-44493

Chemical Property of 4'-Isopropyl-4-biphenylol

Chemical Property:

• Boiling Point: 333.3°Cat760mmHg
• Flash Point: 157.7°C
• PSA: 20.23000
• Density: 1.044g/cm³
• LogP: 4.18260
• XLogP3: 4.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 212.120115130
• Heavy Atom Count: 16
• Complexity: 196

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 4'-Isopropyl-4-biphenylol

There total 2 articles about 4'-Isopropyl-4-biphenylol 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: 71.0%

C27H23S2(1+)*BF4(1-) → p-cumenylphenol (22239-54-9)

Guidance literature:

With 4-oxo-2,2,6,6-tetramethylpiperidin-oxyl; In N,N-dimethyl-formamide; at 20 ℃; for 10h; Inert atmosphere; Sealed tube; UV-irradiation;

DOI:10.1039/d1cc07057f

Reference yield:

4-isopropylbiphenyl (7116-95-2) → p-cumenylphenol (22239-54-9)

Guidance literature:

Multi-step reaction with 2 steps

1: trifluoroacetic anhydride; tetrafluoroboric acid diethyl ether complex / acetonitrile / -40 - 20 °C / 760.05 Torr

2: 4-oxo-2,2,6,6-tetramethylpiperidin-oxyl / N,N-dimethyl-formamide / 10 h / 20 °C / Inert atmosphere; Sealed tube; UV-irradiation

With tetrafluoroboric acid diethyl ether complex; 4-oxo-2,2,6,6-tetramethylpiperidin-oxyl; trifluoroacetic anhydride; In N,N-dimethyl-formamide; acetonitrile;

DOI:10.1039/d1cc07057f

Reference yield:

allyl 1-oxiranylmethylindole-5-carboxylate (1233707-12-4) + p-cumenylphenol (22239-54-9) → C30H31NO4

Guidance literature:

With dmap; at 90 ℃; for 3h; Inert atmosphere;

DOI:10.1021/jm1001088

upstream raw materials:

4-isopropylbiphenyl

Downstream raw materials:

4-n-heptylbenzoic acid 4'-(4-isopropylphenyl)-phenyl ester

4-n-pentylbenzoic acid 4'-(4-isopropylphenyl)-phenyl ester