2-(Methylsulfonyl)benzyl Alcohol

Base Information

Chemical Name:2-(Methylsulfonyl)benzyl Alcohol
CAS No.:864265-08-7
Molecular Formula:C8H10O3S
Molecular Weight:186.232
Hs Code.:2906290090
Mol file:864265-08-7.mol

Synonyms:2-(Methylsulfonyl)benzyl Alcohol;2-(Methylsulfonyl)benzenemethanol

Suppliers and Price of 2-(Methylsulfonyl)benzyl Alcohol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
2-(Methylsulfonyl)benzenemethanol
500mg
$ 1320.00

Medical Isotopes, Inc.
2-(Methylsulfonyl)benzenemethanol
50 mg
$ 650.00

Crysdot
(2-(Methylsulfonyl)phenyl)methanol 97%
5g
$ 475.00

Chemenu
(2-(Methylsulfonyl)phenyl)methanol 95+%
5g
$ 344.00

Ambeed
2-(Methylsulfonyl)benzylAlcohol 98%
1g
$ 154.00

Ambeed
2-(Methylsulfonyl)benzylAlcohol 98%
250mg
$ 68.00

Ambeed
2-(Methylsulfonyl)benzylAlcohol 98%
100mg
$ 46.00

Ambeed
2-(Methylsulfonyl)benzylAlcohol 98%
5g
$ 458.00

Alichem
(2-(Methylsulfonyl)phenyl)methanol
5g
$ 632.42

Alichem
(2-(Methylsulfonyl)phenyl)methanol
1g
$ 215.25

Total 9 raw suppliers

Chemical Property of 2-(Methylsulfonyl)benzyl Alcohol

Chemical Property:

PSA：62.75000
LogP:1.66320
Storage Temp.:2-8°C

Purity/Quality:

97% ^*data from raw suppliers

2-(Methylsulfonyl)benzenemethanol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 2-(Methylsulfonyl)benzyl Alcohol is an intermediate used in the synthetic preparation of thiophene inhibitors of polo-like kinase. 2-(Methylsulfonyl)benzenemethanol is an intermediate used in the synthetic preparation of thiophene inhibitors of polo-like kinase.

Technology Process of 2-(Methylsulfonyl)benzyl Alcohol

There total 3 articles about 2-(Methylsulfonyl)benzyl Alcohol 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:

: 199657-02-8
2-(methylsulfonyl)benzoic acid methyl ester

: 864265-08-7
2-(methanesulfonylphenyl)-methanol

Guidance literature:: With lithium borohydride; In tetrahydrofuran; at 20 - 65 ℃; for 14.75h;

Reference yield:

: 3704-28-7
methyl 2-(methylthio)benzoate

: 864265-08-7
2-(methanesulfonylphenyl)-methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 3-chloro-benzenecarboperoxoic acid / 1,4-dioxane; water / 4 h / 20 °C

2: lithium borohydride / tetrahydrofuran / 14.75 h / 20 - 65 °C

With lithium borohydride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; 1,4-dioxane; water;

Reference yield:

: 4892-02-8
Methyl thiosalicylate

: 864265-08-7
2-(methanesulfonylphenyl)-methanol

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 20 °C

2: 3-chloro-benzenecarboperoxoic acid / 1,4-dioxane; water / 4 h / 20 °C

3: lithium borohydride / tetrahydrofuran / 14.75 h / 20 - 65 °C

With lithium borohydride; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide;