Cas 1268166-99-9,N',N''-dioctyl-N-[(R)-(benzyl)(octyloxycarbonyl)methyl]benzene-1,3,5-tricarboxamide

1268166-99-9

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Basic information

Product Name: N',N''-dioctyl-N-[(R)-(benzyl)(octyloxycarbonyl)methyl]benzene-1,3,5-tricarboxamide
Synonyms: N',N''-dioctyl-N-[(R)-(benzyl)(octyloxycarbonyl)methyl]benzene-1,3,5-tricarboxamide
CAS NO:1268166-99-9
Molecular Formula:
Molecular Weight: 691.995
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',N''-dioctyl-N-[(R)-(benzyl)(octyloxycarbonyl)methyl]benzene-1,3,5-tricarboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N',N''-dioctyl-N-[(R)-(benzyl)(octyloxycarbonyl)methyl]benzene-1,3,5-tricarboxamide(1268166-99-9)
EPA Substance Registry System: N',N''-dioctyl-N-[(R)-(benzyl)(octyloxycarbonyl)methyl]benzene-1,3,5-tricarboxamide(1268166-99-9)

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: 1268166-99-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1268166-99-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,1,6 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1268166-99:
(9*1)+(8*2)+(7*6)+(6*8)+(5*1)+(4*6)+(3*6)+(2*9)+(1*9)=189
189 % 10 = 9
So 1268166-99-9 is a valid CAS Registry Number.

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1268166-99-9Relevant academic research and scientific papers

Sterically demanding benzene-1,3,5-tricarboxamides: Tuning the mechanisms of supramolecular polymerization and chiral amplification

Veld, Martijn A. J.,Haveman, Daniel,Palmans, Anja R. A.,Meijer

, p. 524 - 531 (2011)

Benzene-1,3,5-tricarboxamide (BTA) derivatives with one or three phenylalanine octyl ester (PheOct) moieties were synthesized and their supramolecular polymerization and chiral amplification behavior were investigated in mixing experiments between enantio

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