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trans-3-Hydroxyhex-4-enoic acid

Base Information
  • Chemical Name:trans-3-Hydroxyhex-4-enoic acid
  • CAS No.:26811-78-9
  • Molecular Formula:C6H10O3
  • Molecular Weight:130.142
  • Hs Code.:2918199090
  • European Community (EC) Number:608-000-8
  • Nikkaji Number:J1.881.362I
  • Mol file:26811-78-9.mol
trans-3-Hydroxyhex-4-enoic acid

Synonyms:(E)-3-Hydroxyhex-4-enoic acid;TRANS-3-HYDROXYHEX-4-ENOIC ACID;26811-78-9;81357-32-6;3-HYDROXYHEX-4-ENOIC ACID;13893-40-8;trans-3-Hydroxyhex-4-enoic acid, min. 95 % (1H-NMR);SCHEMBL667905;MFCD09834741;(E)-3-hydroxyhex-4-enoic acid_major;AKOS006328957

Suppliers and Price of trans-3-Hydroxyhex-4-enoic acid
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
  • TRANS-3-HYDROXYHEX-4-ENOIC ACID 95.00%
  • 5MG
  • $ 503.67
Total 3 raw suppliers
Chemical Property of trans-3-Hydroxyhex-4-enoic acid
Chemical Property:
  • PSA:57.53000 
  • LogP:0.39810 
  • XLogP3:-0.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:130.062994177
  • Heavy Atom Count:9
  • Complexity:118
Purity/Quality:

97% *data from raw suppliers

TRANS-3-HYDROXYHEX-4-ENOIC ACID 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC=CC(CC(=O)O)O
  • Isomeric SMILES:C/C=C/C(CC(=O)O)O
Technology Process of trans-3-Hydroxyhex-4-enoic acid

There total 22 articles about trans-3-Hydroxyhex-4-enoic acid 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 sodium hydrogencarbonate; In water; Ambient temperature;
Guidance literature:
N-[(2R,3S)-2-bromo-3-hydroxy-(E)-4-hexenoyl]-(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo[6.2.1.01,5]decane; With water; triethylamine; In dichloromethane; at 0 ℃; for 0.5h;
With aluminium amalgam; In dichloromethane; at 0 ℃; for 0.166667h; Further stages.;
DOI:10.1021/jo000124u
Guidance literature:
With lithium hydroxide; dihydrogen peroxide; In tetrahydrofuran; at 0 ℃; for 3h;
DOI:10.1021/jo00116a011
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