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(R)-1,2-Heptanediol

Base Information Edit
  • Chemical Name:(R)-1,2-Heptanediol
  • CAS No.:78843-64-8
  • Molecular Formula:C7H16 O2
  • Molecular Weight:132.203
  • Hs Code.:
  • European Community (EC) Number:634-757-9
  • DSSTox Substance ID:DTXSID30439142
  • Nikkaji Number:J72.139E
  • Wikidata:Q76415587
  • Mol file:78843-64-8.mol
(R)-1,2-Heptanediol

Synonyms:78843-64-8;(R)-1,2-Heptanediol;SCHEMBL9353298;DTXSID30439142;AG-H-16174

Suppliers and Price of (R)-1,2-Heptanediol
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
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of (R)-1,2-Heptanediol Edit
Chemical Property:
  • PSA:40.46000 
  • LogP:0.91990 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:5
  • Exact Mass:132.115029749
  • Heavy Atom Count:9
  • Complexity:54.9
Purity/Quality:

99%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCC(CO)O
  • Isomeric SMILES:CCCCC[C@H](CO)O
Technology Process of (R)-1,2-Heptanediol

There total 35 articles about (R)-1,2-Heptanediol 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:
With AD-mix-β; In water; tert-butyl alcohol; at 0 ℃; for 120h;
DOI:10.1021/ol500050p
Guidance literature:
With [bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); 3-(2,5-(2R,5R)-dimethylphospholanyl-1)-4-dio-tolylphosphino-2,5-dimethylthiophene; hydrogen bromide; hydrogen; In methanol; at 60 ℃; under 37503.8 Torr; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1002/anie.200902835
Guidance literature:
With osmium(VIII) oxide; (1R,2R)-bis(dimethylamino)cyclohexane; In dichloromethane; for 2h; Mechanism; Ambient temperature; other olefins investigated; enantioselective reaction;
DOI:10.1016/S0040-4039(00)84881-9
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