Cas 1166232-45-6,N<sub>5</sub>-[2-(trifluoroacetylamino)ethylcarbonyl]-N<sub>1</sub>-(tritylaminooxyacetyl)-1,5-diaminonaphthalene

1166232-45-6

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Basic information

Product Name: N₅-[2-(trifluoroacetylamino)ethylcarbonyl]-N₁-(tritylaminooxyacetyl)-1,5-diaminonaphthalene
Synonyms: N₅-[2-(trifluoroacetylamino)ethylcarbonyl]-N₁-(tritylaminooxyacetyl)-1,5-diaminonaphthalene
CAS NO:1166232-45-6
Molecular Formula:
Molecular Weight: 640.662
EINECS: N/A
Product Categories: N/A
Mol File: 1166232-45-6.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: N₅-[2-(trifluoroacetylamino)ethylcarbonyl]-N₁-(tritylaminooxyacetyl)-1,5-diaminonaphthalene(CAS DataBase Reference)
NIST Chemistry Reference: N₅-[2-(trifluoroacetylamino)ethylcarbonyl]-N₁-(tritylaminooxyacetyl)-1,5-diaminonaphthalene(1166232-45-6)
EPA Substance Registry System: N₅-[2-(trifluoroacetylamino)ethylcarbonyl]-N₁-(tritylaminooxyacetyl)-1,5-diaminonaphthalene(1166232-45-6)

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: 1166232-45-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1166232-45-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,6,2,3 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1166232-45:
(9*1)+(8*1)+(7*6)+(6*6)+(5*2)+(4*3)+(3*2)+(2*4)+(1*5)=136
136 % 10 = 6
So 1166232-45-6 is a valid CAS Registry Number.

1166232-45-6Upstream product

1166232-45-6Downstream Products

1166232-46-7 N₅-(2-aminoethylcarbonyl)-N₁-(tritylaminooxyacetyl)-1,5-diaminonaphthalene

1166232-45-6Relevant articles and documents

Construction of highly reactive probes for abasic site detection by introduction of an aromatic and a guanidine residue into an aminooxy group

Kojima, Naoshi,Takebayashi, Toshie,Mikami, Akiko,Ohtsuka, Eiko,Komatsu, Yasuo

, p. 13208 - 13209 (2009)

(Chemical Equation Presented) Abasic sites (AP sites) arise from hydrolysis of glycosidic bonds of DNA that is damaged by various external and internal processes; unrepaired AP sites give rise to genetic mutations. We have constructed highly reactive AP-s

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