4-Hydroxyhexenal

Base Information

Chemical Name:4-Hydroxyhexenal
CAS No.:17427-08-6
Molecular Formula:C₆H₁₀O₂
Molecular Weight:114.144
Hs Code.:2912491000
DSSTox Substance ID:DTXSID701313524
Nikkaji Number:J49.434H,J548.917B
Metabolomics Workbench ID:3415
Mol file:17427-08-6.mol

Synonyms:4-HHE cpd;4-hydroxy-2-hexenal;4-hydroxy-2-hexenal, (E)-isomer;t-4HH;trans-4-hydroxy-2-hexenal

Suppliers and Price of 4-Hydroxyhexenal

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

Total 3 raw suppliers

Chemical Property of 4-Hydroxyhexenal

Chemical Property:

Boiling Point:233.5°Cat760mmHg
Flash Point:94.9°C
PSA：37.30000
Density:0.98g/cm³
LogP:0.51240
XLogP3:0.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:114.068079557
Heavy Atom Count:8
Complexity:86.5

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(C=CC=O)O
Isomeric SMILES:CCC(/C=C/C=O)O

Technology Process of 4-Hydroxyhexenal

There total 10 articles about 4-Hydroxyhexenal 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: 85.0%

: 616-25-1
1-Penten-3-ol

: 107-02-8,25068-14-8
acrolein

: 17427-08-6,150408-28-9,150408-31-4,17427-21-3,160708-91-8
trans-4-hydroxy-2-hexenal

Guidance literature:: With Hoveyda-Grubbs catalyst 2nd generation; In dichloromethane; at 20 ℃; for 20h;
DOI:10.1016/j.chemphyslip.2007.07.003

Reference yield: 72.0%

: 5-ethyl-4-(2-hydroxyethyl)-1,3-dioxolan-2-one

: 17427-08-6,150408-28-9,150408-31-4,17427-21-3,160708-91-8
trans-4-hydroxy-2-hexenal

Guidance literature:: With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In ethyl acetate; for 3h; stereoselective reaction; Inert atmosphere; Reflux;
DOI:10.1002/asia.201900421

Reference yield: 49.0%

: 74-96-4
ethyl bromide

: 18778-96-6,4093-49-6
(2E)-4,4-dimethoxybut-2-enal

: 17427-08-6,150408-28-9,150408-31-4,17427-21-3,160708-91-8
trans-4-hydroxy-2-hexenal

Guidance literature:: ethyl bromide; With magnesium; In diethyl ether;

(2E)-4,4-dimethoxybut-2-enal; In diethyl ether; at 0 - 20 ℃; for 1.5h;
DOI:10.1134/S1070428010030188