AZOXYMETHANE

  • Name: AZOXYMETHANE
  • CAS: 25843-45-2
  • Purity: 99%
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1.What is the AZOXYMETHANE ?

Azoxymethane (AOM), a gene mutation agent, may be used with dextran sulfate sodium (DSS) to create cancer models in laboratory animals which can be used to study mechanisms of cancer progression and chemoprevention.

MeN(<sup>(15)</sup>NO)OH

MeN((15) NO)OH

Azoxymethane
25843-45-2

Azoxymethane

Conditions
Conditions Yield
(<i>Z</i>)-azomethane
4143-42-4,503-28-6

(Z )-azomethane

azoxymethane
54168-20-6,87339-13-7,25843-45-2

azoxymethane

Conditions
Conditions Yield
With Perbenzoic acid;

2.What is the CAS number for AZOXYMETHANE ?

The CAS number of AZOXYMETHANE is 25843-45-2.

More information of AZOXYMETHANE 25843-45-2 are:

CAS?Number

25843-45-2

Density

0.98g/cm3

Boiling Point

92°Cat760mmHg

Flash Point

9.4°C

Vapor Pressure

59.7mmHg at 25°C

Refractive Index

1.4368 (estimate)

HS CODE

2927000090

PSA

41.11000

LogP

0.73170

3.What are another words for AZOXYMETHANE ?

Synonyms?for?AZOXYMETHANE 25843-45-2:Azoxymethane(7CI,8CI); NSC 171779

4.What is the molecular formula of AZOXYMETHANE?

The chemical formula of ?AZOXYMETHANE is?C2H6 N2 O which containing 2 Carbon atoms,6 Hydrogen atoms,2 Nitrogen atoms and 1 Oxygen atoms,and the molecular weight of??AZOXYMETHANE?is 74.0824.

5.What is AZOXYMETHANE (25843-45-2) used for?

Azoxymethane (AOM) is a clear oily liquid that functions as a gene mutation agent. It is primarily utilized in the creation of cancer models in laboratory animals, which aids researchers in studying the mechanisms of cancer progression and exploring potential chemoprevention strategies.

InChI:InChI=1/C2H6N2O/c1-3-4(2)5/h1-2H3/b4-3+

Relevant articles related to AZOXYMETHANE:

Article

Source

Chemistry of unsaturated arenetricarbonylchromium compounds 1. Reaction of (η6-arene)tricarbonylchromium complexes of nitrones with methyl phenylpropiolate

Zarovkina, N. Yu,Sazonova,Artemov,Fukin

, p. 970 - 975 (2015/02/05)

THE FORMATION OF AZOXYALKANES IN REACTIONS OF SOME ORGANOMETALLIC REAGENTS WITH N-nitroso-O,N-DIALKYLHYDROXYLAMINES: THE NONPHOTOCHEMICAL SYNTHESIS OF AN ACYCLIC (E)-AZOXYALKANE

Meesters, A. C. M.,Rueerger, H.,Rajeswari, K.,Benn, M. H.

, p. 264 - 268 (2007/10/02)

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