(3-(2-Chlorophenyl)-5-methylisoxazol-4-yl)methanol

Base Information

Chemical Name:(3-(2-Chlorophenyl)-5-methylisoxazol-4-yl)methanol
CAS No.:495417-33-9
Molecular Formula:C11H10ClNO2
Molecular Weight:223.659
Hs Code.:
DSSTox Substance ID:DTXSID301240915
Mol file:495417-33-9.mol

Synonyms:495417-33-9;(3-(2-Chlorophenyl)-5-methylisoxazol-4-yl)methanol;3-(2-Chlorophenyl)-5-methyl-4-isoxazolemethanol;DTXSID301240915

Suppliers and Price of (3-(2-Chlorophenyl)-5-methylisoxazol-4-yl)methanol

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (3-(2-Chlorophenyl)-5-methylisoxazol-4-yl)methanol

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:223.0400063
Heavy Atom Count:15
Complexity:215

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=NO1)C2=CC=CC=C2Cl)CO

Technology Process of (3-(2-Chlorophenyl)-5-methylisoxazol-4-yl)methanol

There total 5 articles about (3-(2-Chlorophenyl)-5-methylisoxazol-4-yl)methanol 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: 100.0%

: 4357-94-2
methyl 3-(2'-chlorophenyl)-5-methylisoxazole-4-carboxylate

: 495417-33-9
3-(2-chlorophenyl)-5-methylisoxazole-4-carbinol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; at 40 ℃; for 1h;
DOI:10.1055/s-2003-40204

Reference yield: 93.0%

: 83817-50-9
ethyl 3-(2-chlorophenyl)-5-methylisoxazole-4-carboxylate

: 495417-33-9
3-(2-chlorophenyl)-5-methylisoxazole-4-carbinol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃;
DOI:10.1021/jm020354w

Reference yield:

: 29568-74-9
2-chloro-N-hydroxybenzimidoyl chloride

: 495417-33-9
3-(2-chlorophenyl)-5-methylisoxazole-4-carbinol

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaOMe / methanol

1.2: methanol / 4 h / 0 °C

2.1: 100 percent / LiAlH₄ / diethyl ether / 1 h / 40 °C

With lithium aluminium tetrahydride; sodium methylate; In methanol; diethyl ether;
DOI:10.1055/s-2003-40204