54168-20-6 Usage
Description
(E)-1-methoxy-2-methyldiazene, with the molecular formula C3H8N2O and systematic name methoxy(methyl)diazene, is an organic compound featuring a diazene group (N=N) with a methoxy and a methyl group attached. This yellow liquid at room temperature is recognized for its instability and reactivity.
Uses
Used in Organic Synthesis:
(E)-1-methoxy-2-methyldiazene is used as a reagent in the field of organic synthesis for the formation of carbon-carbon bonds, contributing to the creation of various complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (E)-1-methoxy-2-methyldiazene is utilized as a precursor to a range of drugs and biologically active compounds, playing a crucial role in the development of new medications and therapies.
However, it is important to note that due to the unstable nature of (E)-1-methoxy-2-methyldiazene, it requires careful handling and storage to prevent decomposition and potential hazards associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 54168-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,6 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54168-20:
(7*5)+(6*4)+(5*1)+(4*6)+(3*8)+(2*2)+(1*0)=116
116 % 10 = 6
So 54168-20-6 is a valid CAS Registry Number.
54168-20-6Relevant articles and documents
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 reactions of nitrones of the composition (CO)3CrC6H5CH=N+(O-)R (R = Me, Ph, or But) with substituted acetylene were studied. The reactions proceed with high regioselectivity and give 4-
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)
Azoxyalkanes were found to be regiospecifically formed in the reactions of some alkyllithium and Grignard reagents with N-nitroso-O,N-dialkylhydroxylamines.Remarkably, although (Z)-stereomers were usually produced, in one case the (E)-isomer was predominant.
