Cas 1097638-79-3,(E)-2-(7-(3-(4-chlorophenyl)acryloyl)-4,10-dimethyl-1,4,7,10-tetraazacyclododecan-1-yl)-N-cyclohexylacetamide

1097638-79-3

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Basic information

Product Name: (E)-2-(7-(3-(4-chlorophenyl)acryloyl)-4,10-dimethyl-1,4,7,10-tetraazacyclododecan-1-yl)-N-cyclohexylacetamide
Synonyms: (E)-2-(7-(3-(4-chlorophenyl)acryloyl)-4,10-dimethyl-1,4,7,10-tetraazacyclododecan-1-yl)-N-cyclohexylacetamide
CAS NO:1097638-79-3
Molecular Formula:
Molecular Weight: 504.116
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: (E)-2-(7-(3-(4-chlorophenyl)acryloyl)-4,10-dimethyl-1,4,7,10-tetraazacyclododecan-1-yl)-N-cyclohexylacetamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-(7-(3-(4-chlorophenyl)acryloyl)-4,10-dimethyl-1,4,7,10-tetraazacyclododecan-1-yl)-N-cyclohexylacetamide(1097638-79-3)
EPA Substance Registry System: (E)-2-(7-(3-(4-chlorophenyl)acryloyl)-4,10-dimethyl-1,4,7,10-tetraazacyclododecan-1-yl)-N-cyclohexylacetamide(1097638-79-3)

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: 1097638-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1097638-79-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,6,3 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1097638-79:
(9*1)+(8*0)+(7*9)+(6*7)+(5*6)+(4*3)+(3*8)+(2*7)+(1*9)=203
203 % 10 = 3
So 1097638-79-3 is a valid CAS Registry Number.

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1097638-79-3Relevant academic research and scientific papers

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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