3,9-Dioxatricyclo[6.1.0.0~2,4~]nonane

Base Information

Chemical Name:3,9-Dioxatricyclo[6.1.0.0~2,4~]nonane
CAS No.:277-84-9
Molecular Formula:C₇H₁₀O₂
Molecular Weight:126.155
Hs Code.:
DSSTox Substance ID:DTXSID10502626
Nikkaji Number:J1.129.738B
Mol file:277-84-9.mol

Synonyms:277-84-9;3,9-Dioxatricyclo[6.1.0.0~2,4~]nonane;DTXSID10502626

Suppliers and Price of 3,9-Dioxatricyclo[6.1.0.0~2,4~]nonane

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
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price

Total 0 raw suppliers

Chemical Property of 3,9-Dioxatricyclo[6.1.0.0~2,4~]nonane

Chemical Property:

Boiling Point:217.9±8.0 °C(Predicted)
PSA：25.06000
Density:1 +-.0.06 g/cm3(Predicted)
LogP:0.70510
XLogP3:0.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:126.068079557
Heavy Atom Count:9
Complexity:130

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2C(O2)C3C(C1)O3

Technology Process of 3,9-Dioxatricyclo[6.1.0.0~2,4~]nonane

There total 2 articles about 3,9-Dioxatricyclo[6.1.0.0~2,4~]nonane 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: 45.0%

: 6786-21-6
6,7-dioxabicyclo[3.2.2]nona-8-ene

: 277-84-9,72204-20-7
syn-1,2;3,4-diepoxycycloheptane

: 27571-04-6
Cyclohept-2-en-1,4-dion

: 81238-67-7
4-hydroxyl-cyclohept-2-en-1-one

: 53762-86-0
(1R,4S)-cyclohept-2-ene-1,4-diol

Guidance literature:: tetrakis(triphenylphosphine) palladium⁽⁰⁾; In dichloromethane; at 60 ℃; for 29h; Mechanism; variation of amount of catalyst, with and without 2,4,6-tri-t-butylphenol;
DOI:10.1016/S0040-4039(01)82971-3