Cas 796089-76-4,<i>N</i>-{2-[2-(2-amino-ethoxy)-ethoxy]-ethyl}-<i>N</i>'-[1-(4-nitro-phenylcarbamoyl)-2-phenyl-ethyl]-succinamide

796089-76-4

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Basic information

Product Name: N-{2-[2-(2-amino-ethoxy)-ethoxy]-ethyl}-N'-[1-(4-nitro-phenylcarbamoyl)-2-phenyl-ethyl]-succinamide
Synonyms: N-{2-[2-(2-amino-ethoxy)-ethoxy]-ethyl}-N'-[1-(4-nitro-phenylcarbamoyl)-2-phenyl-ethyl]-succinamide
CAS NO:796089-76-4
Molecular Formula:
Molecular Weight: 515.566
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-amino-ethoxy)-ethoxy]-ethyl}-N'-[1-(4-nitro-phenylcarbamoyl)-2-phenyl-ethyl]-succinamide(CAS DataBase Reference)
NIST Chemistry Reference: N-{2-[2-(2-amino-ethoxy)-ethoxy]-ethyl}-N'-[1-(4-nitro-phenylcarbamoyl)-2-phenyl-ethyl]-succinamide(796089-76-4)
EPA Substance Registry System: N-{2-[2-(2-amino-ethoxy)-ethoxy]-ethyl}-N'-[1-(4-nitro-phenylcarbamoyl)-2-phenyl-ethyl]-succinamide(796089-76-4)

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: 796089-76-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 796089-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,6,0,8 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 796089-76:
(8*7)+(7*9)+(6*6)+(5*0)+(4*8)+(3*9)+(2*7)+(1*6)=234
234 % 10 = 4
So 796089-76-4 is a valid CAS Registry Number.

796089-76-4Upstream product

796089-76-4Downstream Products

100-01-6 4-nitro-aniline

796089-76-4Relevant academic research and scientific papers

Monolayer-controlled substrate selectivity using noncovalent enzyme-nanoparticle conjugates

Hong, Rui,Emrick, Todd,Rotello, Vincent M.

, p. 13572 - 13573 (2007/10/03)

Electrostatic interactions were used to noncovalently conjugate chymotrypsin to gold nanoparticles featuring hybrid tetraethylene(glycol)alkanethiol monolayers terminated with carboxylate groups. This conjugation process greatly alters the substrate selectivity of the adsorbed chymotrypsin, inhibiting the hydrolysis of anionic subtrates without affecting the hydrolysis rate of cationic analogues. Copyright

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