Cas 1094756-96-3,N-(tert-butoxycarbonyl)-N'-bis(3,5-di-tert-butylbenzyl)-N''-[4-(pyrid-4-yl)benzyl]guanidine

1094756-96-3

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Basic information

Product Name: N-(tert-butoxycarbonyl)-N'-bis(3,5-di-tert-butylbenzyl)-N''-[4-(pyrid-4-yl)benzyl]guanidine
Synonyms: N-(tert-butoxycarbonyl)-N'-bis(3,5-di-tert-butylbenzyl)-N''-[4-(pyrid-4-yl)benzyl]guanidine
CAS NO:1094756-96-3
Molecular Formula:
Molecular Weight: 528.738
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-(tert-butoxycarbonyl)-N'-bis(3,5-di-tert-butylbenzyl)-N''-[4-(pyrid-4-yl)benzyl]guanidine(CAS DataBase Reference)
NIST Chemistry Reference: N-(tert-butoxycarbonyl)-N'-bis(3,5-di-tert-butylbenzyl)-N''-[4-(pyrid-4-yl)benzyl]guanidine(1094756-96-3)
EPA Substance Registry System: N-(tert-butoxycarbonyl)-N'-bis(3,5-di-tert-butylbenzyl)-N''-[4-(pyrid-4-yl)benzyl]guanidine(1094756-96-3)

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: 1094756-96-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1094756-96-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,4,7,5 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1094756-96:
(9*1)+(8*0)+(7*9)+(6*4)+(5*7)+(4*5)+(3*6)+(2*9)+(1*6)=193
193 % 10 = 3
So 1094756-96-3 is a valid CAS Registry Number.

1094756-96-3Upstream product

1094756-96-3Downstream Products

1094756-96-3Relevant academic research and scientific papers

A guanidinium ion-based anion- and solvent polarity-controllable molecular switch

Lin, Tzu-Chiun,Lai, Chien-Chen,Chiu, Sheng-Hsien

, p. 613 - 616 (2009)

(Chemical Equation Presented) The macrocycle bis-p-xylyl[26]crown-6 (BPX26C6) is capable of complexing guanidinium ions in a [2]pseudorotaxane-like manner in solution. A corresponding molecular switch can be operated through changes in solvent polarity or the addition and removal of halogen and acetate anions.

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