Products Categories
CAS No.: | 837-08-1 |
---|---|
Name: | o-[1-(4-hydroxyphenyl)-1-methylethyl]phenol |
Article Data: | 26 |
Molecular Structure: | |
Formula: | C15H16 O2 |
Molecular Weight: | 228.291 |
Synonyms: | Phenol,2,4'-isopropylidenedi- (8CI); 2,4'-Bisphenol A;2,4'-Dihydroxydiphenyldimethylmethane; 2,4'-Isopropylidenebisphenol;2,4'-Isopropylidenediphenol; 2-(2-Hydroxyphenyl)-2-(4-hydroxyphenyl)propane;4-[2-(2-Hydroxyphenyl)-2-propyl]phenol; o,p-Diphenylolpropane; o,p'-BisphenolA; o,p'-Dian |
Density: | 1.143g/cm3 |
Melting Point: | 110.5 °C |
Boiling Point: | 381.8°C at 760 mmHg |
Flash Point: | 181.5°C |
PSA: | 40.46000 |
LogP: | 3.42370 |
acetone
phenol
A
BPA
B
4-methyl-pent-3-en-2-one
C
2-[1-(4-hydroxyphenyl)-1-methylethyl]-phenol
Conditions | Yield |
---|---|
beta zeolite acidic form at 120℃; under 760.051 Torr; for 12h; | A 63.2% B 0.01% C 11.43% |
acetone
phenol
A
BPA
B
2,2-bis(2-hydroxyphenyl)-propane
C
2-(2-hydroxyphenyl)-2,4,4-trimethylchroman
D
4'-hydroxy-2,4,4-trimethylflavan
E
2-[1-(4-hydroxyphenyl)-1-methylethyl]-phenol
Conditions | Yield |
---|---|
With aluminium(III) phenoxide at 140 - 160℃; for 1h; Product distribution; oth. temperature, oth. ratio of reactants, solvents; | A 8.1% B 1.5% C 7% D 21.6% E 50.3% |
Conditions | Yield |
---|---|
With hydrogenchloride In water at 19.9℃; Rate constant; varying concentrations of reagents; | |
With MCM-41 silica anchored at 70℃; for 24h; Product distribution; Further Variations:; Reagents; Temperatures; atmospheric pressure; | |
With EPMO at 85℃; for 24h; Product distribution; Further Variations:; Reagents; |
methylthiol
acetone
phenol
A
BPA
B
C27H30O3
C
2,2-bis(methylthio)propane
D
2,2-bis(2-hydroxyphenyl)-propane
E
5-hydroxy-3-(4-hydroxyphenyl)-1,1,3-trimethylindane
F
2,4-bis[1-(4-hydroxyphenyl)-1-methylethyl]phenol
G
4-methyl-4-methylthio-2-pentanone
H
2-[1-(4-hydroxyphenyl)-1-methylethyl]-phenol
I
5-hydroxy-1-(4'-hydroxyphenyl)-1,3,3-trimethylindan
Conditions | Yield |
---|---|
strongly acidic 2percent cross linked sulfonated styrene divinylbenzene cationic gel exchange resin CT122 In water at 75℃; for 3h; Product distribution / selectivity; |
2,2-bis(methylthio)propane
acetone
phenol
A
BPA
B
C27H30O3
C
methylthiol
D
2,2-bis(2-hydroxyphenyl)-propane
E
5-hydroxy-3-(4-hydroxyphenyl)-1,1,3-trimethylindane
F
2,4-bis[1-(4-hydroxyphenyl)-1-methylethyl]phenol
G
4-methyl-4-methylthio-2-pentanone
H
2-[1-(4-hydroxyphenyl)-1-methylethyl]-phenol
I
5-hydroxy-1-(4'-hydroxyphenyl)-1,3,3-trimethylindan
Conditions | Yield |
---|---|
strongly acidic 2percent cross linked sulfonated styrene divinylbenzene cationic gel exchange resin CT122 In water at 75℃; for 3h; Product distribution / selectivity; |
acetone
phenol
A
BPA
B
2,2-bis(2-hydroxyphenyl)-propane
C
5-hydroxy-3-(4-hydroxyphenyl)-1,1,3-trimethylindane
D
2,4-bis[1-(4-hydroxyphenyl)-1-methylethyl]phenol
E
2-[1-(4-hydroxyphenyl)-1-methylethyl]-phenol
F
5-hydroxy-1-(4'-hydroxyphenyl)-1,3,3-trimethylindan
Conditions | Yield |
---|---|
Stage #1: phenol With water at 75℃; Autoclave; Stage #2: acetone; 2,2-bis(methylthio)propane In water for 3h; Product distribution / selectivity; | |
Stage #1: phenol With water at 75℃; Autoclave; Stage #2: acetone; methylthiol In water for 3h; Product distribution / selectivity; |
Conditions | Yield |
---|---|
Stage #1: technical CHP; acetone; zirconia, sulfated at 55 - 65℃; Stage #2: phenol at 75℃; for 12h; | A 94 %Chromat. B n/a |
Stage #1: technical CHP; acetone; zirconia, sulfated at 50 - 90℃; under 0 - 517.162 Torr; for 24h; Stage #2: phenol at 75℃; for 12h; | A 92.1 %Chromat. B n/a |
4'-hydroxy-2,4,4-trimethylflavan
phenol
A
BPA
B
2-[1-(4-hydroxyphenyl)-1-methylethyl]-phenol
Conditions | Yield |
---|---|
ion exchange T-66 resin at 93℃; Product distribution / selectivity; |
BPA
2,2,4,4,6,6-hexachloro-1,3,5-triaza-2,4,6-triphosphorine
A
4-isopropenylphenol
B
5-hydroxy-3-(4-hydroxyphenyl)-1,1,3-trimethylindane
C
2,4-bis[1-(4-hydroxyphenyl)-1-methylethyl]phenol
D
2-[1-(4-hydroxyphenyl)-1-methylethyl]-phenol
E
phenol
Conditions | Yield |
---|---|
With potassium carbonate In chlorobenzene at 170℃; for 2h; |