7-(1,3-Dioxolan-2-yl)-2,6-dimethyl-2-heptanol

Base Information

Chemical Name:7-(1,3-Dioxolan-2-yl)-2,6-dimethyl-2-heptanol
CAS No.:5309-57-9
Molecular Formula:C₆H₈O₂
Molecular Weight:112.128
Hs Code.:
DSSTox Substance ID:DTXSID30385635
Nikkaji Number:J404.267K
Mol file:5309-57-9.mol

Synonyms:AC1MDPBT;CBMicro_016899;Oprea1_244397;DTXSID30385635;CCG-5741;BIM-0016717.P001;AB00079968-01;7-(1,3-Dioxolan-2-yl)-2,6-dimethyl-2-heptanol

Suppliers and Price of 7-(1,3-Dioxolan-2-yl)-2,6-dimethyl-2-heptanol

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

TRC
cis,trans-SorbicAcid
25mg
$ 215.00

Total 3 raw suppliers

Chemical Property of 7-(1,3-Dioxolan-2-yl)-2,6-dimethyl-2-heptanol

Chemical Property:

Vapor Pressure:0.000152mmHg at 25°C
Melting Point:35 - 38°C
Boiling Point:296°Cat760mmHg
Flash Point:147.6°C
Density:0.975g/cm³
Storage Temp.:Amber Vial, Refrigerator, Under inert atmosphere
Solubility.:Chloroform (Slightly), Methanol (Slightly)
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:216.17254462
Heavy Atom Count:15
Complexity:174

Purity/Quality:: cis,trans-SorbicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CCCC(C)(C)O)CC1OCCO1
Uses cis,trans-Sorbic acid has been used in the study of photosensitization of carbon nanotubes and the production of reactive oxygen species by using the sorbic acid as a catalyst in the reaction process.

Technology Process of 7-(1,3-Dioxolan-2-yl)-2,6-dimethyl-2-heptanol

There total 17 articles about 7-(1,3-Dioxolan-2-yl)-2,6-dimethyl-2-heptanol 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: 79.0%

: 4423-18-1
(but-2-enylidene)malonic acid

: 110-44-1,5309-56-8,5309-57-9,22500-92-1,30361-30-9,91751-55-2
(2Z,4E)-hexa-2,4-dienoic acid

Guidance literature:: With quinoline; at 130 ℃; for 3h;
DOI:10.1021/ja020635t

Reference yield: 54.0%

: 3-butenoic acid 1-methyl-2-propen-1-yl ester

: 110-44-1,5309-56-8,5309-57-9,22500-92-1,30361-30-9,91751-55-2
(2Z,4E)-hexa-2,4-dienoic acid

Guidance literature:: With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; sodium hydride; In toluene; mineral oil; at 65 ℃; for 4.5h;
DOI:10.1002/anie.202106250