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100046-25-1

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100046-25-1 Usage

Chemical structure

The compound has a diene ring containing both silicon and nitrogen atoms, as well as methyl and phenyl groups at various positions.

Potential applications

Materials science, organic synthesis, and pharmaceutical research.

Reactivity

The compound has potential reactivity due to its unique structure.

Further study needed

More research is required to fully understand the potential uses and properties of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 100046-25-1 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 100046-25:
(8*1)+(7*0)+(6*0)+(5*0)+(4*4)+(3*6)+(2*2)+(1*5)=51
51 % 10 = 1
So 100046-25-1 is a valid CAS Registry Number.

100046-25-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methyl-2,2,6-triphenyl-1,4-di-p-tolyl-1,2-dihydro-[1,3,2]diazasiline

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100046-25-1 SDS

100046-25-1Relevant articles and documents

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

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