2,4-Dibenzyloxybenzyl Alcohol

Base Information

Chemical Name:2,4-Dibenzyloxybenzyl Alcohol
CAS No.:33617-58-2
Molecular Formula:C21H20O3
Molecular Weight:320.388
Hs Code.:
DSSTox Substance ID:DTXSID10441889
Nikkaji Number:J846.247J
Wikidata:Q82258886
Mol file:33617-58-2.mol

Synonyms:2,4-Dibenzyloxybenzyl Alcohol;33617-58-2;[2,4-bis(phenylmethoxy)phenyl]methanol;Benzenemethanol, 2,4-bis(phenylmethoxy)-;(2,4-bis(benzyloxy)phenyl)methanol;MFCD08456666;[2,4-bis(benzyloxy)phenyl]methanol;2,4-DibenzyloxybenzylAlcohol;SCHEMBL7907404;DTXSID10441889;2,4-Bis(benzyloxy)benzyl alcohol;XPKZCTCRUPIJEF-UHFFFAOYSA-N;(2,4-bis-benzyloxyphenyl)methanol;AKOS005291298;AS-32123;SY024921;CS-0436711;FT-0703148;A875234

Suppliers and Price of 2,4-Dibenzyloxybenzyl 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

Crysdot
2,4-DIBENZYLOXYBENZYLALCOHOL 95+%
5g
$ 350.00

Crysdot
2,4-DIBENZYLOXYBENZYLALCOHOL 95+%
1g
$ 160.00

Chemenu
2,4-DIBENZYLOXYBENZYLALCOHOL 95%
10g
$ 438.00

AK Scientific
2,4-Dibenzyloxybenzylalcohol
250mg
$ 131.00

Total 5 raw suppliers

Chemical Property of 2,4-Dibenzyloxybenzyl Alcohol

Chemical Property:

PSA：38.69000
LogP:4.33690
Storage Temp.:Sealed in dry,Room Temperature
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:320.14124450
Heavy Atom Count:24
Complexity:334

Purity/Quality:

97% ^*data from raw suppliers

2,4-DIBENZYLOXYBENZYLALCOHOL 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=CC(=C(C=C2)CO)OCC3=CC=CC=C3

Technology Process of 2,4-Dibenzyloxybenzyl Alcohol

There total 5 articles about 2,4-Dibenzyloxybenzyl 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: 99.0%

: 13246-46-3
2,4-dibenzyloxybenzaldehyde

: 33617-58-2
2,4-dibenzyloxybenzyl alcohol

Guidance literature:: With sodium tetrahydroborate; In methanol; Ambient temperature;
DOI:10.1016/S0040-4039(00)96340-8

Reference yield:

: 95-01-2
2,4-Dihydroxybenzaldehyde

: 33617-58-2
2,4-dibenzyloxybenzyl alcohol

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / K₂CO₃ / dimethylformamide / 18 h / Ambient temperature

2: 26 percent / NaBH₄ / methanol / 0.08 h

With sodium tetrahydroborate; potassium carbonate; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0223-5234(97)81678-9

Reference yield:

: 100-39-0
benzyl bromide

: 33617-58-2
2,4-dibenzyloxybenzyl alcohol

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / K₂CO₃ / dimethylformamide / 18 h / Ambient temperature

2: 26 percent / NaBH₄ / methanol / 0.08 h

With sodium tetrahydroborate; potassium carbonate; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0223-5234(97)81678-9