Product Name

  • Name

    2-ETHYLBENZYL ALCOHOL 98

  • EINECS
  • CAS No. 767-90-8
  • Article Data40
  • CAS DataBase
  • Density 1.00 g/cm3
  • Solubility
  • Melting Point
  • Formula C9H12O
  • Boiling Point 229.3 °C at 760 mmHg
  • Molecular Weight 136.194
  • Flash Point 106.1 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 767-90-8 (2-ETHYLBENZYL ALCOHOL  98)
  • Hazard Symbols
  • Synonyms 2-ETHYLBENZYL ALCOHOL 98
  • PSA 20.23000
  • LogP 1.74130

Synthetic route

2-ethylbenzaldehyde
22927-13-5

2-ethylbenzaldehyde

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
With sodium tetrahydroborate In ethanol for 4h; Reduction; Heating;99%
With sodium tetrahydroborate In ethanol at 0 - 25℃; for 2h;74%
With sodium tetrahydroborate In methanol Heating;
2-ethylbenzoic acid
612-19-1

2-ethylbenzoic acid

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
With diborane In tetrahydrofuran at 0 - 20℃; for 24h;87%
With diborane In tetrahydrofuran; methanol at 0 - 20℃; for 24h;87%
Stage #1: 2-ethylbenzoic acid With boron trifluoride diethyl etherate In tetrahydrofuran at 0 - 20℃; for 24h;
Stage #2: With methanol In tetrahydrofuran for 0.75h;
87%
2-ethynylbenzyl alcohol
10602-08-1

2-ethynylbenzyl alcohol

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
With hydrogen In glycerol at 100℃; under 2250.23 Torr; for 24h; chemoselective reaction;84%
2-acetyl-benzoic acid
577-56-0

2-acetyl-benzoic acid

A

3-methylphthalide
3453-64-3

3-methylphthalide

B

1-(1-hydroxyethyl)-2-hydroxymethylbenzene
57259-71-9

1-(1-hydroxyethyl)-2-hydroxymethylbenzene

C

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
With samarium diiodide; water In tetrahydrofuran for 0.0333333h; Ambient temperature;A 41%
B 36%
C 11%
2-methyl-benzyl alcohol
89-95-2

2-methyl-benzyl alcohol

methyl iodide
74-88-4

methyl iodide

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
Stage #1: 2-methyl-benzyl alcohol With n-butyllithium In diethyl ether; hexane for 4h; Heating;
Stage #2: methyl iodide In diethyl ether; hexane at 20℃; for 1h;
33%
ethanol
64-17-5

ethanol

phenyldiazomethane
908094-04-2

phenyldiazomethane

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

formaldehyd
50-00-0

formaldehyd

2-ethylphenylmagnesium bromide
21450-63-5

2-ethylphenylmagnesium bromide

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
With diethyl ether
ethanol
64-17-5

ethanol

N-benzyl-N-nitrosobenzamide
10575-94-7

N-benzyl-N-nitrosobenzamide

A

benzoic acid benzyl ester
120-51-4

benzoic acid benzyl ester

B

N-benzylbenzamide
1485-70-7

N-benzylbenzamide

C

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

D

benzoic acid
65-85-0

benzoic acid

Conditions
ConditionsYield
weitere Produkten: Benzylamin,Aethylnitrit,salpetrige Saeure;
diethyl ether
60-29-7

diethyl ether

benzyl bromide
100-39-0

benzyl bromide

orthoformic acid diethyl ester; sodium-compound

orthoformic acid diethyl ester; sodium-compound

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

sodium phenoxide
139-02-6

sodium phenoxide

benzyl potassium
2785-29-7

benzyl potassium

ethyl ester of p-toluenesulfonic acid
80-40-0

ethyl ester of p-toluenesulfonic acid

A

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

B

Phenetole
103-73-1

Phenetole

formaldehyd
50-00-0

formaldehyd

ethylbenzene
100-41-4

ethylbenzene

A

(RS)-2-phenyl-1-propanol
1123-85-9

(RS)-2-phenyl-1-propanol

B

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
multistep reaction; optional ortho and alpha hydroxymethylation of alkylarenes;
Yield given. Multistep reaction. Yields of byproduct given;
2-ethylbenzyl chloride
1467-06-7

2-ethylbenzyl chloride

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

2-ethylbenzoyl chloride
76118-05-3

2-ethylbenzoyl chloride

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
With lithium aluminium tetrahydride
1,3-dihydroisobenzofuran
496-14-0

1,3-dihydroisobenzofuran

methyl iodide
74-88-4

methyl iodide

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
With naphthalene; lithium 1.) THF, 0 deg C, 2 h, 2.) THF, -10 deg C, 60 min; Yield given. Multistep reaction;
With naphthalene; lithium 1) THF, 0 deg C, 1.5 h, 2) THF, 0 deg C, 60 min; Yield given. Multistep reaction;
1,3-dihydro-1-methylisobenzofuran
38189-85-4

1,3-dihydro-1-methylisobenzofuran

A

1-O-tolyl-ethanol
7287-82-3

1-O-tolyl-ethanol

B

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
With naphthalene; water; lithium 1) THF, 0 deg C, 3 h; Yield given. Multistep reaction. Yields of byproduct given;
benzyl chloride
100-44-7

benzyl chloride

alcoholic KOH-solution

alcoholic KOH-solution

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

ethanol
64-17-5

ethanol

benzyl chloride
100-44-7

benzyl chloride

zinc dust

zinc dust

A

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

B

toluene
108-88-3

toluene

benzyl chloride
100-44-7

benzyl chloride

alcoholic potassium acetate

alcoholic potassium acetate

A

Benzyl acetate
140-11-4

Benzyl acetate

B

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

C

benzyl alcohol
100-51-6

benzyl alcohol

sulfuric acid
7664-93-9

sulfuric acid

2-ethylbenzoic acid
612-19-1

2-ethylbenzoic acid

lead-cathode

lead-cathode

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
bei der elektrolytischen Reduktion;
benzyl iodoethyl ether
54555-84-9

benzyl iodoethyl ether

diethyl ether
60-29-7

diethyl ether

magnesium

magnesium

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
nachfolgend Zersetzung;
(diethoxymethyl)benzene
774-48-1

(diethoxymethyl)benzene

hydrogen

hydrogen

used nickel catalyst

used nickel catalyst

A

ethanol
64-17-5

ethanol

B

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
at 180℃;
ethanol
64-17-5

ethanol

N,N,N-tribenzyl methylammonium iodide
18265-23-1

N,N,N-tribenzyl methylammonium iodide

sodium amalgam

sodium amalgam

A

N-methyldibenzylamine
102-05-6

N-methyldibenzylamine

B

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

ethanol
64-17-5

ethanol

allyl-dibenzyl-methyl-ammonium; iodide
111413-94-6

allyl-dibenzyl-methyl-ammonium; iodide

sodium amalgam

sodium amalgam

A

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

B

N-allyl-N-α-methylbenzylamine
2520-97-0

N-allyl-N-α-methylbenzylamine

ethanol
64-17-5

ethanol

benzyldimethylphenylammonium chloride
3204-68-0

benzyldimethylphenylammonium chloride

sodium

sodium

A

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

B

N,N-dimethyl-aniline
121-69-7

N,N-dimethyl-aniline

1,3-dihydroisobenzofuran
496-14-0

1,3-dihydroisobenzofuran

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1) sec-BuLi / 1) THF, -40 deg C, 2 h, 2) THF, 1 h
2: 1) Li, naphthalene, 2) H2O / 1) THF, 0 deg C, 3 h
View Scheme
ortho-ethylaniline
578-54-1

ortho-ethylaniline

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: NaBH4 / methanol / Heating
View Scheme
1-bromo-2-ethylbenzene
1973-22-4

1-bromo-2-ethylbenzene

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1.) magnesium / 1.) ether
2: LiAlH4 / diethyl ether
View Scheme
ethylbenzene
100-41-4

ethylbenzene

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 16.8 percent / SnCl4 / CHCl3
View Scheme
2-Ethyltoluene
611-14-3

2-Ethyltoluene

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

Conditions
ConditionsYield
With Cellulosimicrobium cellulans EB-8-4 at 30℃; for 10h; pH=7; Microbiological reaction; K-buffer containing glucose; Enzymatic reaction; regioselective reaction;94 %Chromat.
N,N-diisopropylcarbamoyl chloride
19009-39-3

N,N-diisopropylcarbamoyl chloride

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

2-ethylbenzyl N,N-diisopropylcarbamate
1086338-61-5

2-ethylbenzyl N,N-diisopropylcarbamate

Conditions
ConditionsYield
Stage #1: (2-ethylphenyl)methanol With sodium hydride In tetrahydrofuran; mineral oil at 0℃; Inert atmosphere;
Stage #2: N,N-diisopropylcarbamoyl chloride In tetrahydrofuran; mineral oil at 20℃; for 48h; Inert atmosphere;
98%
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

1-(bromomethyl)-2-ethylbenzene
57825-29-3

1-(bromomethyl)-2-ethylbenzene

Conditions
ConditionsYield
With phosphorus tribromide In diethyl ether at 20℃; for 0.166667h;94%
With bromine; triphenylphosphine In dichloromethane Bromination; Heating;80%
With hydrogen bromide
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

allyl bromide
106-95-6

allyl bromide

1-allyloxymethyl-2-ethylbenzene

1-allyloxymethyl-2-ethylbenzene

Conditions
ConditionsYield
Stage #1: (2-ethylphenyl)methanol With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.5h;
Stage #2: allyl bromide In tetrahydrofuran; mineral oil at 0 - 20℃;
90%
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

benzoyl chloride
98-88-4

benzoyl chloride

2-ethylbenzyl benzoate
1070881-24-1

2-ethylbenzyl benzoate

Conditions
ConditionsYield
With pyridine at 0℃; for 1.5h;89%
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

p-benzoquinone
106-51-4

p-benzoquinone

4-hydroxyphenyl 2-ethylbenzoate

4-hydroxyphenyl 2-ethylbenzoate

Conditions
ConditionsYield
With tert.-butylhydroperoxide; copper(II) acetate monohydrate In water; dimethyl sulfoxide at 100 - 110℃; for 20h; Sealed tube;68%
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

2-ethylbenzoic acid
612-19-1

2-ethylbenzoic acid

Conditions
ConditionsYield
With oxygen; eosin y In acetonitrile at 20℃; Irradiation;65%
(Z)-1-bromo-2-(triisopropylsilyloxymethyl)but-2-ene
1044749-61-2

(Z)-1-bromo-2-(triisopropylsilyloxymethyl)but-2-ene

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

(E)-1-(2-ethylbenzyloxy)-2-(triisopropylsilyloxymethyl)but-2-ene
1044750-04-0

(E)-1-(2-ethylbenzyloxy)-2-(triisopropylsilyloxymethyl)but-2-ene

Conditions
ConditionsYield
With potassium tert-butylate In tetrahydrofuran at 20℃; for 16h;63%
4-amino-2-methylpyrimidine-5-carbaldehyde
73-68-7

4-amino-2-methylpyrimidine-5-carbaldehyde

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

2-Methyl-6-(2-trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine
76574-74-8

2-Methyl-6-(2-trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine

Conditions
ConditionsYield
With sodium ethanolate In ethanol for 4h; Heating;45%
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

3-(2-((triethylsilyl)peroxy)propan-2-yl)cyclohexanone

3-(2-((triethylsilyl)peroxy)propan-2-yl)cyclohexanone

(±)-(1R*,5S*)-1-((2-ethylbenzyl)oxy)-4,4-dimethyl-2,3-dioxabicyclo[3.3.1]nonane

(±)-(1R*,5S*)-1-((2-ethylbenzyl)oxy)-4,4-dimethyl-2,3-dioxabicyclo[3.3.1]nonane

Conditions
ConditionsYield
With toluene-4-sulfonic acid In dichloromethane at 25℃;30%
naphthalene
91-20-3

naphthalene

(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

1-Benzyl-naphthalene
611-45-0

1-Benzyl-naphthalene

Conditions
ConditionsYield
With phosphorus pentoxide
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

methylmagnesium bromide
75-16-1

methylmagnesium bromide

ethylbenzene
100-41-4

ethylbenzene

Conditions
ConditionsYield
at 160 - 180℃;
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

anthracene
120-12-7

anthracene

Conditions
ConditionsYield
With phosphorus pentaoxide
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

1-Phenyl-1-propanol
93-54-9

1-Phenyl-1-propanol

Conditions
ConditionsYield
With sodium at 130 - 210℃;
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

2-ethylbenzaldehyde
22927-13-5

2-ethylbenzaldehyde

Conditions
ConditionsYield
With chromium(III) oxide; sulfuric acid
With chromium(VI) oxide; silica gel In diethyl ether; dichloromethane for 24h;
With dipyridinium dichromate; trichloroacetic acid In acetonitrile at 19.99℃; Kinetics; Further Variations:; Temperatures;
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

Conditions
ConditionsYield
With iodine; chlorine
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

2-ethylbenzyl chloride
1467-06-7

2-ethylbenzyl chloride

Conditions
ConditionsYield
With thionyl chloride; N,N-diethylaniline
With thionyl chloride
With thionyl chloride In benzene Heating;
With thionyl chloride In benzene
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

acetic acid
64-19-7

acetic acid

acetic acid-(2-ethyl-benzyl ester)
100058-58-0

acetic acid-(2-ethyl-benzyl ester)

Conditions
ConditionsYield
With potassium acetate
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

toluene
108-88-3

toluene

1-methyl-4-(phenylmethyl)benzene
620-83-7

1-methyl-4-(phenylmethyl)benzene

Conditions
ConditionsYield
With tin(IV) chloride
With phosphorus pentoxide
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

benzene
71-43-2

benzene

Diphenylmethane
101-81-5

Diphenylmethane

Conditions
ConditionsYield
With titanium tetrachloride
With aluminium trichloride
(2-ethylphenyl)methanol
767-90-8

(2-ethylphenyl)methanol

benzene
71-43-2

benzene

anthracene
120-12-7

anthracene

Conditions
ConditionsYield
With aluminium trichloride

2-Ethylbenzyl alcohol Specification

This chemical is called (2-Ethylphenyl)methanol, and it can also be named as 2-Ethylbenzyl alcohol. With the molecular formula of C9H12O, its product categories are Alcohols; C9 to C30; Oxygen Compounds. The CAS registry number of this chemical is 767-90-8. In addition, this chemical should be sealed in the ventilated and dry place, away from light.

Other characteristics of the (2-Ethylphenyl)methanol can be summarised as followings: (1)ACD/LogP: 2.03; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.03; (4)ACD/LogD (pH 7.4): 2.03; (5)ACD/BCF (pH 5.5): 20.41; (6)ACD/BCF (pH 7.4): 20.41; (7)ACD/KOC (pH 5.5): 301.4; (8)ACD/KOC (pH 7.4): 301.4; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 3; (12)Polar Surface Area: 9.23 Å2; (13)Index of Refraction: 1.533; (14)Molar Refractivity: 42.25 cm3; (15)Molar Volume: 136 cm3; (16)Polarizability: 16.75×10-24cm3; (17)Surface Tension: 37.8 dyne/cm; (18)Density: 1 g/cm3; (19)Flash Point: 106.1 °C; (20)Enthalpy of Vaporization: 49.24 kJ/mol; (21)Boiling Point: 229.3 °C at 760 mmHg; (22)Vapour Pressure: 0.0393 mmHg at 25°C.

You can still convert the following datas into molecular structure: 
1.SMILES: OCc1ccccc1CC
2.InChI: InChI=1/C9H12O/c1-2-8-5-3-4-6-9(8)7-10/h3-6,10H,2,7H2,1H3
3.InChIKey: SBUIQTMDIOLKAL-UHFFFAOYAQ

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