Cas 1096706-40-9,N-(2-(1H-imidazol-1-yl)ethyl)-N-(2,4-dichlorobenzyl)-2-(1H-imidazol-1-yl)ethanamine

1096706-40-9

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Basic information

Product Name: N-(2-(1H-imidazol-1-yl)ethyl)-N-(2,4-dichlorobenzyl)-2-(1H-imidazol-1-yl)ethanamine
Synonyms: N-(2-(1H-imidazol-1-yl)ethyl)-N-(2,4-dichlorobenzyl)-2-(1H-imidazol-1-yl)ethanamine
CAS NO:1096706-40-9
Molecular Formula:
Molecular Weight: 364.277
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(2-(1H-imidazol-1-yl)ethyl)-N-(2,4-dichlorobenzyl)-2-(1H-imidazol-1-yl)ethanamine(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-(1H-imidazol-1-yl)ethyl)-N-(2,4-dichlorobenzyl)-2-(1H-imidazol-1-yl)ethanamine(1096706-40-9)
EPA Substance Registry System: N-(2-(1H-imidazol-1-yl)ethyl)-N-(2,4-dichlorobenzyl)-2-(1H-imidazol-1-yl)ethanamine(1096706-40-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1096706-40-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1096706-40-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,6,7,0 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1096706-40:
(9*1)+(8*0)+(7*9)+(6*6)+(5*7)+(4*0)+(3*6)+(2*4)+(1*0)=169
169 % 10 = 9
So 1096706-40-9 is a valid CAS Registry Number.

1096706-40-9Upstream product

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1096706-40-9Relevant academic research and scientific papers

Synthesis and biological activities of novel amine-derived bis-azoles as potential antibacterial and antifungal agents

Fang, Bo,Zhou, Cheng-He,Rao, Xian-Cai

experimental part, p. 4388 - 4398 (2010/10/02)

A series of novel amine-derived bis-azole compounds were designed by the systematical structural modification of Fluconazole and synthesized by a convenient and efficient method, and the antimicrobial activities for all prepared compounds were evaluated i

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