100046-26-2 Usage
Silacyclic compound
Contains a six-membered ring structure with a silicon atom and two nitrogen atoms.
Cyclohexyl group
A six-membered carbon ring with one carbon atom replaced by a silicon atom.
Methyl group
A single carbon atom (-CH3) attached to the ring structure.
Tetraphenyl
Four phenyl groups (C6H5) attached to the ring structure.
Potential applications
Organic synthesis and materials science.
Unique structure
The combination of a silacyclic ring, cyclohexyl group, methyl group, and four phenyl groups provides a distinct chemical structure.
Chemical properties
The compound's properties are influenced by its molecular structure, including its reactivity, stability, and solubility.
Check Digit Verification of cas no
The CAS Registry Mumber 100046-26-2 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 100046-26:
(8*1)+(7*0)+(6*0)+(5*0)+(4*4)+(3*6)+(2*2)+(1*6)=52
52 % 10 = 2
So 100046-26-2 is a valid CAS Registry Number.
100046-26-2Relevant 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
