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(4R)-5-(Phenylmethoxy)-1,4-pentanediol

Base Information Edit
  • Chemical Name:(4R)-5-(Phenylmethoxy)-1,4-pentanediol
  • CAS No.:93381-43-2
  • Molecular Formula:C12H18O3
  • Molecular Weight:210.273
  • Hs Code.:
  • DSSTox Substance ID:DTXSID501281951
  • Mol file:93381-43-2.mol
(4R)-5-(Phenylmethoxy)-1,4-pentanediol

Synonyms:93381-43-2;(4R)-5-(Phenylmethoxy)-1,4-pentanediol;DTXSID501281951

Suppliers and Price of (4R)-5-(Phenylmethoxy)-1,4-pentanediol
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 0 raw suppliers
Chemical Property of (4R)-5-(Phenylmethoxy)-1,4-pentanediol Edit
Chemical Property:
  • XLogP3:1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:7
  • Exact Mass:210.125594432
  • Heavy Atom Count:15
  • Complexity:144
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)COCC(CCCO)O
  • Isomeric SMILES:C1=CC=C(C=C1)COC[C@@H](CCCO)O
Technology Process of (4R)-5-(Phenylmethoxy)-1,4-pentanediol

There total 5 articles about (4R)-5-(Phenylmethoxy)-1,4-pentanediol 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:
Guidance literature:
(R)-1-benzyloxypent-4-en-2-ol; With dimethylsulfide borane complex; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
With sodium hydroxide; dihydrogen peroxide; In tetrahydrofuran; water; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1002/chem.200801024
Guidance literature:
With methanol; lithium borohydride; In tetrahydrofuran; at 0 - 5 ℃; for 16h; Inert atmosphere;
DOI:10.1002/anie.200805241
Guidance literature:
Multi-step reaction with 2 steps
1: 74 percent / trifluoromethanesulfonic acid / CH2Cl2; pentane / 0.5 h / 0 °C
2: DIBAL / toluene / 1 h / -78 °C
With trifluorormethanesulfonic acid; diisobutylaluminium hydride; In dichloromethane; toluene; pentane;
DOI:10.1021/ja000001r
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