Cas 915951-06-3,Acetamide, N-[(2S)-3-[bis(4-methoxyphenyl)phenylmethoxy]-2-hydroxypropyl]-2,2,2- trifluoro-N-[2-(1H-indol-3-yl)ethyl]-

915951-06-3

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Basic information

Product Name: Acetamide, N-[(2S)-3-[bis(4-methoxyphenyl)phenylmethoxy]-2-hydroxypropyl]-2,2,2- trifluoro-N-[2-(1H-indol-3-yl)ethyl]-
Synonyms:
CAS NO:915951-06-3
Molecular Formula: C36H35F3N2O5
Molecular Weight: 632.68
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: Acetamide, N-[(2S)-3-[bis(4-methoxyphenyl)phenylmethoxy]-2-hydroxypropyl]-2,2,2- trifluoro-N-[2-(1H-indol-3-yl)ethyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Acetamide, N-[(2S)-3-[bis(4-methoxyphenyl)phenylmethoxy]-2-hydroxypropyl]-2,2,2- trifluoro-N-[2-(1H-indol-3-yl)ethyl]-(915951-06-3)
EPA Substance Registry System: Acetamide, N-[(2S)-3-[bis(4-methoxyphenyl)phenylmethoxy]-2-hydroxypropyl]-2,2,2- trifluoro-N-[2-(1H-indol-3-yl)ethyl]-(915951-06-3)

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: 915951-06-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915951-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,9,5 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 915951-06:
(8*9)+(7*1)+(6*5)+(5*9)+(4*5)+(3*1)+(2*0)+(1*6)=183
183 % 10 = 3
So 915951-06-3 is a valid CAS Registry Number.

915951-06-3Upstream product

3389-21-7 3-(2-bromoethyl)-1H-indole

915951-06-3Downstream Products

915951-06-3Relevant academic research and scientific papers

Indole as an artificial DNA base incorporated via an acyclic 2′-deoxyriboside substitute

Wanninger, Claudia,Wagenknecht, Hans-Achim

, p. 2051 - 2054 (2008/02/05)

Indole was synthetically incorporated into DNA as an artificial base at specific sites of duplex DNA. An acyclic substitute for the 2′-deoxyribose was applied in order to obtain a chemically stable nucleoside analogue that can be synthesized by a fast and

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