4-bromo-2-{[(5-methyl-3-isoxazolyl)imino]methyl}phenol

Base Information

Chemical Name:4-bromo-2-{[(5-methyl-3-isoxazolyl)imino]methyl}phenol
CAS No.:88812-68-4
Molecular Formula:C11H9BrN2O2
Molecular Weight:281.10500
Hs Code.:
Mol file:88812-68-4.mol

Synonyms:4-Bromo-2-{[(E)-5-methyl-isoxazol-3-ylimino]-methyl}-phenol;3-(2-hydroxy-5-bromobenzylideneamino)-5-methylisoxazole;

Suppliers and Price of 4-bromo-2-{[(5-methyl-3-isoxazolyl)imino]methyl}phenol

Supply Marketing:

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

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Chemical Property of 4-bromo-2-{[(5-methyl-3-isoxazolyl)imino]methyl}phenol

Chemical Property:

Melting Point:110 - 112 °C (Petroleum ether)
PSA：58.62000
LogP:3.20170

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of 4-bromo-2-{[(5-methyl-3-isoxazolyl)imino]methyl}phenol

There total 1 articles about 4-bromo-2-{[(5-methyl-3-isoxazolyl)imino]methyl}phenol 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%

: 1072-67-9
5-methylisoxazol-3-ylamine

: 1761-61-1
5-bromosalicyclaldehyde

: 88812-68-4
4-bromo-2-[(5-methyl-3-isoxazolyl)imino]methylphenol

Guidance literature:: Reflux;

Reference yield: 80.0%

: 88812-68-4
4-bromo-2-[(5-methyl-3-isoxazolyl)imino]methylphenol

: 1153622-51-5
4-bromo-2-[(5-methyl-3-isoxazolyl)amino]methylphenol

Guidance literature:: With sodium tetrahydroborate; In ethanol; at 20 ℃; for 0.5h;
DOI:10.1002/jhet.38

Reference yield:

: 88812-68-4
4-bromo-2-[(5-methyl-3-isoxazolyl)imino]methylphenol

: 1233715-09-7
C₁₉H₁₈BrN₃O₃

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate

2: chloroform / 6 h / 90 °C

With sodium tetrahydroborate; In chloroform;