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Name |
Triphenylmethanol |
EINECS | 200-988-5 |
CAS No. | 76-84-6 | Density | 1.13 g/cm3 |
PSA | 20.23000 | LogP | 3.97080 |
Solubility | insoluble in water | Melting Point |
160-163 °C(lit.) |
Formula | C19H16O | Boiling Point | 380 °C at 760 mmHg |
Molecular Weight | 260.335 | Flash Point | 168.7 °C |
Transport Information | N/A | Appearance | white powder |
Safety | 22-24/25-36-26 | Risk Codes | 36/37/38 |
Molecular Structure | Hazard Symbols | Xi | |
Synonyms |
Methanol,triphenyl- (8CI);BL 3756;Hydroxytriphenylmethane;NSC 4050;Triphenylcarbinol;Triphenylmethyl alcohol;Tritanol;Tritylalcohol;U 45483;a,a-Diphenylbenzenemethanol; |
Article Data | 607 |
Conditions | Yield |
---|---|
With water In tetrachloromethane | 100% |
With water Kinetics; Rate constant; Mechanism; Two-phase systems; | |
With water In acetone at 25℃; Kinetics; ΔS, ΔH (excit.); |
bromo-triphenyl-methane
di-sec-butyl mercury
A
triphenylmethyl alcohol
B
secondary-butyl mercury(II) bromide
C
sec-butyl triphenylmethyl peroxide
Conditions | Yield |
---|---|
With oxygen; tetrabutylammomium bromide In 1,2-dichloro-ethane; benzene Product distribution; other reaction conditions; | A n/a B n/a C 100% |
With oxygen; tetrabutylammomium bromide In 1,2-dichloro-ethane Yields of byproduct given; | A n/a B n/a C 76% |
trimethylsilyl triphenyl methyl ether
triphenylmethyl alcohol
Conditions | Yield |
---|---|
Stage #1: trimethylsilyl triphenyl methyl ether With nitrogen dioxide at 20℃; for 0.833333h; Stage #2: With water | 100% |
With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0833333h; Green chemistry; | 99% |
With montmorillonite K-10 In methanol for 4h; Ambient temperature; | 98% |
triphenylmethyl alcohol
Conditions | Yield |
---|---|
With acid-washed bentonite In acetone at 40 - 50℃; for 0.166667h; | 100% |
Conditions | Yield |
---|---|
With chromyl chloride In tetrachloromethane at 22℃; for 0.5h; ultrasound sonication; | 99% |
With potassium hydroxide; 18-crown-6 ether; oxygen; dimethyl sulfoxide In 1,2-dimethoxyethane at 20℃; for 1.5h; | 97% |
With chromium(VI) oxide; tetrabutylammonium periodite In dichloromethane; acetonitrile at -40℃; for 0.166667h; | 97% |
1-diphenylmethylene-4-trityl-2,5-cyclohexadiene
A
triphenylmethyl alcohol
Conditions | Yield |
---|---|
In tetrahydrofuran; acetonitrile at 20℃; for 0.5h; Reagent/catalyst; Inert atmosphere; Glovebox; | A 99% B 83% |
4,5-dihydroxymethyl-1-triphenylmethylimidazole
A
4,5-dihydroxymethylimidazole
B
triphenylmethyl alcohol
Conditions | Yield |
---|---|
With acetic acid for 1.5h; Heating; | A 98.5% B n/a |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid at 50℃; for 12h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
In water at 25℃; for 0.00555556h; Solvent; | 98% |
Conditions | Yield |
---|---|
With potassium 12-tungstocobaltate(III) In water; acetonitrile for 0.2h; Microwave irradiation; | 96% |
With 1H-imidazole; C17H16ClMnN2O2; tetrabutylammonium periodite In chloroform at 20℃; for 0.333333h; | 95% |
With oxygen; mercury(II) oxide In methanol; acetonitrile at 25℃; UV-irradiation; | 88% |
Triphenylmethanol is also known as Trityl alcohol, Triphenylcarbinol, 76-84-6, Methanol, triphenyl-, Tritanol, Triphenylmethyl alcohol, triphenylmethan-1-ol. With the Molecular Formula C19H16O, it is an organic compound and a white crystalline solid that is insoluble in water and petroleum ether, but well soluble in ethanol, diethyl ether, and benzene. It reacts with acetyl chloride to give triphenylmethyl chloride.
Physical properties about Triphenylmethanol are: (1)ACD/LogP: 3.836; (2)ACD/LogD (pH 5.5): 3.84; (3)ACD/LogD (pH 7.4): 3.84; (4)ACD/BCF (pH 5.5): 484.72; (5)ACD/BCF (pH 7.4): 484.71; (6)ACD/KOC (pH 5.5): 2909.88; (7)ACD/KOC (pH 7.4): 2909.86; (8)#H bond acceptors: 1; (9)#H bond donors: 1; (10)#Freely Rotating Bonds: 4; (11)Index of Refraction: 1.622; (12)Molar Refractivity: 81.072 cm3; (13)Molar Volume: 230.289 cm3; (14)Polarizability: 32.14 10-24cm3; (15)Surface Tension: 46.4389991760254 dyne/cm; (16)Density: 1.13 g/cm3; (17)Flash Point: 168.744 °C; (18)Enthalpy of Vaporization: 66.255 kJ/mol; (19)Boiling Point: 379.999 °C at 760 mmHg
Preparation of Triphenylmethanol: The preparation of triphenylmethanol from methyl benzoate or benzophenone and bromobenzene is a common laboratory experiment for teaching the Grignard reaction. An alternative starting material is diethyl carbonate.
When you are using this chemical, please be cautious about it as the following:
1. Do not breathe dust;
2. Avoid contact with skin and eyes;
3. Wear suitable protective clothing;
4. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice;
You can still convert the following datas into molecular structure:
(1)InChI=1S/C19H16O/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,20H;
(2)InChIKey=LZTRCELOJRDYMQ-UHFFFAOYSA-N;
(3)SmilesC(c1ccccc1)(c1ccccc1)(c1ccccc1)O;