(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methanol

Base Information

Chemical Name:(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methanol
CAS No.:70502-03-3
Molecular Formula:C11H11 N O2
Molecular Weight:189.214
Hs Code.:2934999090
European Community (EC) Number:640-820-1
DSSTox Substance ID:DTXSID30468750
Nikkaji Number:J1.651.123D
Wikidata:Q82296128
Mol file:70502-03-3.mol

Synonyms:(5-methyl-2-phenyl-1,3-oxazol-4-yl)methanol;70502-03-3;(5-methyl-2-phenyloxazol-4-yl)methanol;(5-methyl-2-phenyl-oxazol-4-yl)-methanol;4-(Hydroxymethyl)-5-methyl-2-phenyl-1,3-oxazole;[5-methyl-2-phenyl-1,3-oxazol-4-yl]methanol;4-Oxazolemethanol,5-methyl-2-phenyl-;SCHEMBL4037331;DTXSID30468750;AAQIALLSQXGHHT-UHFFFAOYSA-N;MFCD08271881;5-methyl-2-phenyl-4-oxazolylmethanol;AKOS006343021;5-methyl-2-phenyl-4-oxazolyl methanol;AS-6547;(5-methyl-2-phenyl-4-oxazolyl)methanol;CS-0322589;FT-0719865;J-501599

Suppliers and Price of (5-Methyl-2-phenyl-1,3-oxazol-4-yl)methanol

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

SynQuest Laboratories
4-(Hydroxymethyl)-5-methyl-2-phenyl-1,3-oxazole 95%
1 g
$ 570.00

Matrix Scientific
(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methanol
10g
$ 2430.00

Matrix Scientific
(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methanol
5g
$ 1530.00

Matrix Scientific
(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methanol
1g
$ 720.00

Apolloscientific
4-(Hydroxymethyl)-5-methyl-2-phenyl-1,3-oxazole 95%
1g
$ 356.00

American Custom Chemicals Corporation
(5-METHYL-2-PHENYL-1,3-OXAZOL-4-YL)METHANOL 95.00%
1G
$ 848.96

Advanced Chemicals Intermediatesced Chemicals Intermediates
(5-Methyl-2-phenyl-oxazol-4-yl)-methanol 95%+
5g
$ 1225.25

Advanced Chemicals Intermediatesced Chemicals Intermediates
(5-Methyl-2-phenyl-oxazol-4-yl)-methanol 95%+
1g
$ 355.25

Acints
(5-Methyl-2-phenyl-oxazol-4-yl)-methanol 95%+
1g
$ 355.25

Total 7 raw suppliers

Chemical Property of (5-Methyl-2-phenyl-1,3-oxazol-4-yl)methanol

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:117 °C
Boiling Point:361.125°C at 760 mmHg
Flash Point:172.202°C
PSA：46.26000
Density:1.176g/cm³
LogP:2.14230
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:189.078978594
Heavy Atom Count:14
Complexity:180

Purity/Quality:

98%min ^*data from raw suppliers

4-(Hydroxymethyl)-5-methyl-2-phenyl-1,3-oxazole 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(N=C(O1)C2=CC=CC=C2)CO

Technology Process of (5-Methyl-2-phenyl-1,3-oxazol-4-yl)methanol

There total 6 articles about (5-Methyl-2-phenyl-1,3-oxazol-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: 92.0%

: 70502-03-3
[5-methyl-2-phenyl-1,3-oxazol-4-yl]methanol

Guidance literature:

Reference yield: 84.0%

: 61151-96-0
ethyl 5-methyl-2-phenyloxazole-4-carboxylate

: 70502-03-3
[5-methyl-2-phenyl-1,3-oxazol-4-yl]methanol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; for 1h; Ambient temperature;
DOI:10.1021/jm00088a022

Reference yield:

: ethyl 5-methyl-3-oxo-2-phenyloxazole-4-carboxylate hydrochloride

: 70502-03-3
[5-methyl-2-phenyl-1,3-oxazol-4-yl]methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 40 percent / H₂ / 10percent Pd/C / ethanol; methanol / 3 h / 2585.7 Torr

2: 84 percent / LiAlH₄ / diethyl ether / 1 h / Ambient temperature

With lithium aluminium tetrahydride; hydrogen; palladium on activated charcoal; In methanol; diethyl ether; ethanol;
DOI:10.1021/jm00088a022