Cas 1097638-57-7,N-cyclohexyl-2-(methyl(2-(methyl(2-(N-methylacetamido)ethyl)amino)ethyl)amino)acetamide

1097638-57-7

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Basic information

Product Name: N-cyclohexyl-2-(methyl(2-(methyl(2-(N-methylacetamido)ethyl)amino)ethyl)amino)acetamide
Synonyms: N-cyclohexyl-2-(methyl(2-(methyl(2-(N-methylacetamido)ethyl)amino)ethyl)amino)acetamide
CAS NO:1097638-57-7
Molecular Formula:
Molecular Weight: 326.483
EINECS: N/A
Product Categories: N/A
Mol File: 1097638-57-7.mol
Article Data: 1

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-cyclohexyl-2-(methyl(2-(methyl(2-(N-methylacetamido)ethyl)amino)ethyl)amino)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-cyclohexyl-2-(methyl(2-(methyl(2-(N-methylacetamido)ethyl)amino)ethyl)amino)acetamide(1097638-57-7)
EPA Substance Registry System: N-cyclohexyl-2-(methyl(2-(methyl(2-(N-methylacetamido)ethyl)amino)ethyl)amino)acetamide(1097638-57-7)

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: 1097638-57-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1097638-57-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,6,3 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1097638-57:
(9*1)+(8*0)+(7*9)+(6*7)+(5*6)+(4*3)+(3*8)+(2*5)+(1*7)=197
197 % 10 = 7
So 1097638-57-7 is a valid CAS Registry Number.

1097638-57-7Upstream product

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1097638-57-7Relevant articles and documents

Direct preparation of unsymmetrical difunctionalized cyclen derivatives by an ugi multicomponent reaction

Piersanti, Giovanni,Remi, Francesco,Fusi, Vieri,Formica, Mauro,Giorgi, Luca,Zappia, Giovanni

supporting information; experimental part, p. 417 - 420 (2009/07/18)

(Chemical Equation Presented) A new and efficient synthetic protocol for the preparation of unsymmetrical difunctionalized cyclen and its close derivatives using a modified Ugi reaction (N-split Ugi) is described. The scope of this methodology is further

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