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HEXAMETHYLENE OXIDE
  • Chemical Name: HEXAMETHYLENE OXIDE
  • CAS No.: 592-90-5

HEXAMETHYLENE OXIDE GMP Manufacturer Global Trade 592-90-5 with Fast Delivery

  • Molecular Formula: C6H12 O
  • Molecular Weight: 100.161
  • Vapor Pressure: 17.1mmHg at 25°C 
  • Refractive Index: 1.4390 
  • Boiling Point: 122°Cat760mmHg 
  • Flash Point: 14.2°C 
  • PSA： 9.23000 
  • Density: 0.869g/cm3 
  • LogP: 1.57700 

HEXAMETHYLENE OXIDE(Cas 592-90-5) Usage

Definition

ChEBI: A saturated organic heteromonocyclic parent that is cycloheptane in which one of the methylene groups is replaced by oxygen.

InChI:InChI=1/C6H12O/c1-2-4-6-7-5-3-1/h1-6H2

592-90-5 Relevant articles

Silver(I)-Catalyzed Reductive Cross-Coupling of Aldehydes to Structurally Diverse Cyclic and Acyclic Ethers

Dong, Guichao,Li, Chuang,Liang, Ting,Xu, Xin,Xu, Zhou

supporting information, p. 1817 - 1821 (2022/03/16)

A range of medium-sized cyclic ethers (5...

Ring-Closing Metathesis of Aliphatic Ethers and Esterification of Terpene Alcohols Catalyzed by Functionalized Biochar

Kerton, Francesca M.,MacQuarrie, Stephanie L.,Vidal, Juliana L.,Wyper, Olivia M.

supporting information, p. 6052 - 6056 (2021/12/10)

Functionalized biochars, renewable carbo...

Synthetic method of epoxide

-

Paragraph 0020; 0034; 0035; 0036, (2018/10/11)

The invention discloses a synthetic meth...

Remarkably high catalyst efficiency of a disilaruthenacyclic complex for hydrosilane reduction of carbonyl compounds

Tahara, Atsushi,Sunada, Yusuke,Takeshita, Takashi,Inoue, Ryoko,Nagashima, Hideo

supporting information, p. 11192 - 11195 (2018/10/24)

A disilaruthenacyclic complex (1) showed...

592-90-5 Process route

1,2-epoxy-5-hexene
10353-53-4

1,2-epoxy-5-hexene

oxepane
592-90-5

oxepane

2,5-dimethyltetrahydrofuran
1003-38-9

2,5-dimethyltetrahydrofuran

2-methyloxane
10141-72-7

2-methyloxane

Conditions
Conditions Yield
With bromine; tri-n-butyl-tin hydride; Yield given. Multistep reaction. Yields of byproduct given; 1.) carbon tetrachloride, rt. 2 h.; 2.) ether, reflux, 24 h.;
1,6-hexanediol
629-11-8

1,6-hexanediol

oxepane
592-90-5

oxepane

hexahydro-2H-oxepin-2-one
502-44-3,24980-41-4,80137-66-2

hexahydro-2H-oxepin-2-one

1,5-Hexadien
592-42-7

1,5-Hexadien

1,4-hexadiene
592-45-0

1,4-hexadiene

hex-4-en-1-ol
6126-50-7,928-91-6,928-92-7

hex-4-en-1-ol

cyclohexane
110-82-7,25012-93-5

cyclohexane

1-amino-cyclopentanemethanol
3637-61-4

1-amino-cyclopentanemethanol

cyclohexene
110-83-8

cyclohexene

cyclohexanol
108-93-0

cyclohexanol

Conditions
Conditions Yield
With aluminum oxide; In ethanol; at 300 ℃; for 5h; Inert atmosphere;

592-90-5 Upstream products

  • 629-11-8
    629-11-8

    1,6-hexanediol

  • 4286-55-9
    4286-55-9

    1-bromo-6-hexanol

  • 50592-87-5
    50592-87-5

    1-bromo-6-methoxyhexane

  • 10353-53-4
    10353-53-4

    1,2-epoxy-5-hexene

592-90-5 Downstream products

  • 26306-01-4
    26306-01-4

    6-iodo-1-(trimethylsilyloxy)hexane

  • 96185-58-9
    96185-58-9

    Trimethyl-(6-phenyltellanyl-hexyloxy)-silane

  • 108584-85-6
    108584-85-6

    (4aR,8S,8aS)-7-Chloro-8-nitro-2-phenyl-4,4a,8,8a-tetrahydro-pyrano[3,2-d][1,3]dioxine

  • 87960-91-6
    87960-91-6

    (4aR,6R,7R,8S,8aS)-6,7-Dichloro-8-nitro-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine

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