2-HEXANONE OXIME

  • CAS：5577-48-0
  • purity：99%
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Details

Good factory supply good 2-HEXANONE OXIME 5577-48-0

  • Molecular Formula: C6H13NO
  • Molecular Weight: 115.175
  • Vapor Pressure: 0.282mmHg at 25°C 
  • Refractive Index: 1.435 
  • Boiling Point: 187.5 °C at 760 mmHg 
  • Flash Point: 94 °C 
  • PSA： 32.59000 
  • Density: 0.89 g/cm3 
  • LogP: 2.02670 

2-HEXANONE OXIME(Cas 5577-48-0) Usage

General Description

2-HEXANONE OXIME is a chemical compound with the molecular formula C6H13NO. It is a colorless to pale yellow liquid with a sharp, sweet, and floral odor. 2-HEXANONE OXIME is commonly used as an intermediate in the synthesis of various chemicals and pharmaceuticals. It is also utilized as a chemical intermediate in the production of pesticides and herbicides. Additionally, 2-HEXANONE OXIME has properties that make it useful in the formulation of coatings, adhesives, and sealants. However, exposure to 2-HEXANONE OXIME can cause eye and skin irritation, and it may be harmful if inhaled or ingested. Therefore, appropriate precautions should be taken when handling this chemical.

InChI:InChI=1/C6H13NO/c1-3-4-5-6(2)7-8/h8H,3-5H2,1-2H3/b7-6-

5577-48-0 Relevant articles

Arylboronic Acid-Catalyzed C-Allylation of Unprotected Oximes: Total Synthesis of N-Me-Euphococcine

Kürti, László,Kattamuri, Padmanabha V.,Siitonen, Juha H.,Yousufuddin, Muhammed

supporting information, (2020/03/24)

O-Unprotected keto-and aldoximes are rea...

Iminyl Radical-Triggered Intermolecular Distal C(sp3)-H Heteroarylation via 1,5-Hydrogen-Atom Transfer (HAT) Cascade

Gu, Yu-Rui,Duan, Xin-Hua,Chen, Li,Ma, Zhi-Yong,Gao, Pin,Guo, Li-Na

supporting information, p. 917 - 920 (2019/02/14)

An efficient iron-catalyzed intermolecul...

Iminyl Radical-Mediated Controlled Hydroxyalkylation of Remote C(sp3)-H Bond via Tandem 1,5-HAT and Difunctionalization of Aryl Alkenes

Ma, Zhi-Yong,Guo, Li-Na,Gu, Yu-Rui,Chen, Li,Duan, Xin-Hua

supporting information, p. 4341 - 4347 (2018/10/20)

A visible-light mediated γ-hydroxyalkyla...

5577-48-0 Process route

hexane
110-54-3

hexane

2-chlorohexane
638-28-8

2-chlorohexane

Hexan-2-on-oxim
5577-48-0,97421-49-3,97421-52-8

Hexan-2-on-oxim

propyl ethyl ketoxime
28364-56-9

propyl ethyl ketoxime

1-Chlorohexane
544-10-5

1-Chlorohexane

Conditions
Conditions Yield
With hydrogenchloride; nitrosylchloride; at 20 ℃; for 9h; Further byproducts given; Irradiation;
n-hexan-2-one
591-78-6

n-hexan-2-one

Hexan-2-on-oxim
5577-48-0,97421-49-3,97421-52-8

Hexan-2-on-oxim

Conditions
Conditions Yield
With sodium hydroxide; hydroxylamine;
With hydroxylamine hydrochloride; sodium acetate; In ethanol; water; at 70 ℃; for 3h;
With hydroxylamine hydrochloride; sodium acetate; In ethanol; water; at 100 ℃; Irradiation;

5577-48-0 Upstream products

  • 110-54-3
    110-54-3

    hexane

  • 591-78-6
    591-78-6

    n-hexan-2-one

5577-48-0 Downstream products

  • 19692-48-9
    19692-48-9

    Butyl-methyl-ketonoxim-pikrylether

  • 70492-67-0
    70492-67-0

    (S)-hexan-2-amine

  • 5329-79-3
    5329-79-3

    (R)‐2‐aminohexane

  • 591-78-6
    591-78-6

    n-hexan-2-one

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