100046-23-9 Usage
Chemical structure
A complex organic compound with a silicon atom in the ring structure.
Composition
Contains four phenyl groups, a methyl group, and a 1,3-diaza group.
1,3-Diaza group
Consists of two nitrogen atoms separated by a carbon atom.
Aromatic rings
Presence of multiple aromatic rings in the structure.
Reactivity
Highly reactive due to the presence of multiple aromatic rings and the silicon atom.
Potential applications
Useful in various chemical applications, such as inorganic synthesis and materials science.
Research and experimentation
Further research and experimentation are needed to fully understand the properties and potential uses of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 100046-23-9 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 100046-23:
(8*1)+(7*0)+(6*0)+(5*0)+(4*4)+(3*6)+(2*2)+(1*3)=49
49 % 10 = 9
So 100046-23-9 is a valid CAS Registry Number.
100046-23-9Relevant academic research and scientific papers
Barluenga, Jose,Tomas, Miguel,Ballesteros, Alfredo,Gotor, Vicente
, p. 489 - 490 (1987)
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
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
