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cis-4-Cyclopentene-1,3-Diol

Base Information Edit
  • Chemical Name:cis-4-Cyclopentene-1,3-Diol
  • CAS No.:29783-26-4
  • Molecular Formula:C5H8O2
  • Molecular Weight:100.117
  • Hs Code.:2906190090
  • European Community (EC) Number:627-215-8
  • Nikkaji Number:J253.410J
  • Mol file:29783-26-4.mol
cis-4-Cyclopentene-1,3-Diol

Synonyms:29783-26-4;cis-4-Cyclopentene-1,3-Diol;cis-3,5-Dihydroxy-1-cyclopentene;cis-cyclopent-4-ene-1,3-diol;(1R,3S)-CYCLOPENT-4-ENE-1,3-DIOL;4-Cyclopentene-1,3-diol, (1R,3S)-rel-;4-Cyclopentene-1,3-diol, cis-;(1S,3R)-cyclopent-4-ene-1,3-diol;(1R,3S)-rel-cyclopent-4-ene-1,3-diol;694-47-3;SCHEMBL255121;cis-2-Cyclopentene-1,4-Diol;cis-cyclopent-2-ene-1,4-diol;cis-Cyclopent-1-ene-3,5-diol;2-Cyclopentene-1beta,4beta-diol;cis-cyclopent-4-ene-1, 3-diol;4-Cyclopentene-1,3-diol, (Z)-;MFCD00077703;AKOS015855423;AS-50388;BP-21428;CS-0056064;P10067;cis-4-Cyclopentene-1,3-diol, >=99.0% (GC);J-017636

Suppliers and Price of cis-4-Cyclopentene-1,3-Diol
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
  • SynQuest Laboratories
  • cis-4-Cyclopentene-1,3-diol
  • 100 mg
  • $ 157.00
  • Sigma-Aldrich
  • cis-4-Cyclopentene-1,3-diol ≥99.0% (GC)
  • 500mg
  • $ 147.00
  • Sigma-Aldrich
  • cis-4-Cyclopentene-1,3-diol ≥99.0% (GC)
  • 2.5g
  • $ 682.00
  • Crysdot
  • cis-Cyclopent-4-ene-1,3-diol 97%
  • 1g
  • $ 600.00
  • Biosynth Carbosynth
  • cis-4-Cyclopentene-1,3-diol
  • 500 mg
  • $ 200.00
  • Biosynth Carbosynth
  • cis-4-Cyclopentene-1,3-diol
  • 1 g
  • $ 350.00
  • Biosynth Carbosynth
  • cis-4-Cyclopentene-1,3-diol
  • 250 mg
  • $ 125.00
  • Biosynth Carbosynth
  • cis-4-Cyclopentene-1,3-diol
  • 100 mg
  • $ 70.00
  • Biosynth Carbosynth
  • cis-4-Cyclopentene-1,3-diol
  • 50 mg
  • $ 50.00
  • Apolloscientific
  • cis-4-Cyclopentene-1,3-diol
  • 100mg
  • $ 143.00
Total 41 raw suppliers
Chemical Property of cis-4-Cyclopentene-1,3-Diol Edit
Chemical Property:
  • Vapor Pressure:0.014mmHg at 25°C 
  • Melting Point:56-59 °C 
  • Refractive Index:1.596 
  • Boiling Point:229.157 °C at 760 mmHg 
  • PKA:14.01±0.40(Predicted) 
  • Flash Point:113.673 °C 
  • PSA:40.46000 
  • Density:1.318 g/cm3 
  • LogP:-0.33190 
  • XLogP3:-0.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:100.052429494
  • Heavy Atom Count:7
  • Complexity:78.1
Purity/Quality:

98%,99%, *data from raw suppliers

cis-4-Cyclopentene-1,3-diol *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1C(C=CC1O)O
  • Isomeric SMILES:C1[C@H](C=C[C@H]1O)O
  • Uses cis-4-Cyclopentene-1,3-diol is an important building block for the synthesis of natural products with cyclopentanoid structure elements. It was used in preparation of key intermediates of prostaglandin synthesis.
Technology Process of cis-4-Cyclopentene-1,3-Diol

There total 31 articles about cis-4-Cyclopentene-1,3-Diol 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 oxygen; rose bengal; thiourea; In methanol; at 20 ℃; for 12h; Irradiation;
DOI:10.3987/COM-08-S(F)59
Guidance literature:
With potassium carbonate; In methanol; at 0 ℃; for 4h;
DOI:10.1055/s-2007-967937
Guidance literature:
With tris(triphenylphosphine)ruthenium(II) chloride; In dichloromethane; at -25 ℃; for 1h; Product distribution; ruthenium(II) catalyzed reaction of 1,4-endoperoxide;
DOI:10.1021/ja00371a041
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