100046-22-8 Usage
Chemical structure
Contains a silicon atom, a nitrogen atom, and a six-membered ring structure.
Substituents
Includes five methyl groups and five phenyl groups attached to the ring.
Application
Used in the field of chemistry for its unique properties and potential applications in catalysis, organic synthesis, and material science.
Potential uses
May have potential uses in the development of new pharmaceuticals or advanced materials due to its distinctive structure and reactivity.
Further research
Further research and testing would be needed to fully understand its potential uses and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 100046-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,4 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100046-22:
(8*1)+(7*0)+(6*0)+(5*0)+(4*4)+(3*6)+(2*2)+(1*2)=48
48 % 10 = 8
So 100046-22-8 is a valid CAS Registry Number.
100046-22-8Relevant academic research and scientific papers
Reactivity of the nitrogen-silicon bond. Pyridines and furo[2,3-b][1,4]diazepines from 4-amino-1-azabutadienes via 1,2-dihydro-1,3,2-diazasilines
Barluenga,Tomas,Ballesteros,Kong
, p. 106 - 112 (2007/10/02)
1,2-Dihydro-1,3,2-diazasilines 2 are prepared from 4-amino-1-azadienes 1 and react with dialkyl acetylenedicarboxylates to produce six- and seven-membered heterocycles depending on the substitution pattern of 1. Highly functionalized pyridine-2-carboxylat
A Simple Synthesis of Substituted 2-Imino-1,2-dihydropyrimidines From 1-Azabutadienes via Diazasilines
Barluenga, Jose,Tomas, Miguel,Ballesteros, Alfredo,Gotor, Vicente
, p. 489 - 490 (2007/10/02)
1,2-Dihydro-1,3,2-diazasilines, formed on reaction of 4-amino-1-azabutadienes (3-amino-2-propenylideneamines) with dichlorodiphenyl- or dichlorodimethylsilane, react with aliphatic and aromatic isocyanates to give high yields of substituted 2-imino-1,2-di
