2-Phenyltetrahydro-2H-pyran-4-OL

Base Information

Chemical Name:2-Phenyltetrahydro-2H-pyran-4-OL
CAS No.:82065-19-8
Molecular Formula:C11H14 O2
Molecular Weight:178.231
Hs Code.:2932999099
DSSTox Substance ID:DTXSID80438160
Nikkaji Number:J1.058.242C
Mol file:82065-19-8.mol

Synonyms:2-PHENYLTETRAHYDRO-2H-PYRAN-4-OL;2-phenyloxan-4-ol;132149-01-0;82065-19-8;2-phenyl-tetrahydro-2H-pyran-4-ol;2-phenyl-tetrahydro-pyran-4-ol;2-phenyltetrahydropyran-4-ol;SCHEMBL1265907;DTXSID80438160;MFCD12025409;AKOS013422757;CCG-358802;SB45941;SB47533;AS-40369;FT-0772995;FT-0773663;EN300-116011;A840242;2H-Pyran-4-ol,tetrahydro-2-phenyl-,(2R,4S)-rel-;F8880-4174;Z1192341080

Suppliers and Price of 2-Phenyltetrahydro-2H-pyran-4-OL

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

American Custom Chemicals Corporation
2-PHENYLTETRAHYDRO-2H-PYRAN-4-OL 95.00%
5MG
$ 505.22

AK Scientific
2-Phenyltetrahydro-2H-pyran-4-ol
10g
$ 4220.00

AK Scientific
2-Phenyltetrahydro-2H-pyran-4-ol
1g
$ 1081.00

AK Scientific
2-Phenyltetrahydro-2H-pyran-4-ol
250mg
$ 519.00

Total 7 raw suppliers

Chemical Property of 2-Phenyltetrahydro-2H-pyran-4-OL

Chemical Property:

PSA：29.46000
LogP:1.89900
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:178.099379685
Heavy Atom Count:13
Complexity:152

Purity/Quality:

97% ^*data from raw suppliers

2-PHENYLTETRAHYDRO-2H-PYRAN-4-OL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1COC(CC1O)C2=CC=CC=C2

Technology Process of 2-Phenyltetrahydro-2H-pyran-4-OL

There total 10 articles about 2-Phenyltetrahydro-2H-pyran-4-OL 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%

: 627-27-0
homoalylic alcohol

: 100-52-7
benzaldehyde

: 82065-19-8
cis-2-phenyl-4-hydroxy-tetrahydropyran

Guidance literature:: With phosphomolybdic acid; In water; at 23 ℃; for 8h;
DOI:10.1055/s-2007-1000932

Reference yield: 82.0%

: 132148-94-8
1-Phenyl-5-tributylstannanyl-pentane-1,3-diol

: 82065-19-8,82065-23-4,82110-16-5,82110-20-1,132149-01-0
2-phenyltetrahydro-2H-pyran-4-ol

Guidance literature:: With lead(IV) acetate; In benzene; for 2h; Ambient temperature;
DOI:10.1039/c39900001492

Reference yield: 82.0%

: 546-67-8
lead(IV) tetraacetate

: 132148-94-8
1-Phenyl-5-tributylstannanyl-pentane-1,3-diol

: 82065-19-8,82065-23-4,82110-16-5,82110-20-1,132149-01-0
2-phenyltetrahydro-2H-pyran-4-ol

Guidance literature:: In benzene; A mixture of the diol and LTA in dry benzene is stirred at room temp. under N2 for 2 h.; quenching (saturated NH4Cl), removal of aq. layer and extracting (CHCl3), drying of combined org. layers (anhyd. MgSO4), concn., purifn. by silica column chromy. (n-hexane-ethyl acetate) as eluant;
DOI:10.1039/c39900001492