Cas 1039151-75-1,N-(2-{2-[2-(2-aminoethoxy)ethoxy]ethoxy}ethyl)-4-(1-hydroxyethyl)-3-nitrobenzamide

1039151-75-1

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Basic information

Product Name: N-(2-{2-[2-(2-aminoethoxy)ethoxy]ethoxy}ethyl)-4-(1-hydroxyethyl)-3-nitrobenzamide
Synonyms: N-(2-{2-[2-(2-aminoethoxy)ethoxy]ethoxy}ethyl)-4-(1-hydroxyethyl)-3-nitrobenzamide
CAS NO:1039151-75-1
Molecular Formula:
Molecular Weight: 385.417
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-(2-{2-[2-(2-aminoethoxy)ethoxy]ethoxy}ethyl)-4-(1-hydroxyethyl)-3-nitrobenzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-{2-[2-(2-aminoethoxy)ethoxy]ethoxy}ethyl)-4-(1-hydroxyethyl)-3-nitrobenzamide(1039151-75-1)
EPA Substance Registry System: N-(2-{2-[2-(2-aminoethoxy)ethoxy]ethoxy}ethyl)-4-(1-hydroxyethyl)-3-nitrobenzamide(1039151-75-1)

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: 1039151-75-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1039151-75-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,9,1,5 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1039151-75:
(9*1)+(8*0)+(7*3)+(6*9)+(5*1)+(4*5)+(3*1)+(2*7)+(1*5)=131
131 % 10 = 1
So 1039151-75-1 is a valid CAS Registry Number.

1039151-75-1Upstream product

1039152-01-6 N-(2-{2-[2-(2-azidoethoxy)ethoxy]ethoxy}ethyl)-4-(1-hydroxyethyl)-3-nitrobenzamide

1039151-75-1Downstream Products

1039151-82-0 4-(1-hydroxyethyl)-3-nitro-N-{2-[2-(2-{2-[4-(4-oxopentanoylamino)benzoylamino]ethoxy}ethoxy)ethoxy]ethyl}benzamide

1039151-75-1Relevant academic research and scientific papers

Photocleavable initiator nucleotide substrates for an aldolase ribozyme

Fusz, Stefan,Srivatsan, Seergazhi G.,Ackermann, Damian,Famulok, Michael

, p. 5069 - 5077 (2008/12/20)

(Chemical Equation Presented) We have previously reported the in vitro selection of a ribozyme that catalyzes an aldol reaction between a levulinic amide aldol donor and a benzaldehyde substrate. The selection scheme involved the priming of the RNA librar

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