Cas 90362-80-4,N-{3-[2-(2,2-Diethoxy-ethyl)-6-prop-(Z)-ylidene-3,6-dihydro-2H-pyridin-1-yl]-3-oxo-propyl}-4-methyl-benzenesulfonamide

90362-80-4

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Basic information

Product Name: N-{3-[2-(2,2-Diethoxy-ethyl)-6-prop-(Z)-ylidene-3,6-dihydro-2H-pyridin-1-yl]-3-oxo-propyl}-4-methyl-benzenesulfonamide
Synonyms: N-{3-[2-(2,2-Diethoxy-ethyl)-6-prop-(Z)-ylidene-3,6-dihydro-2H-pyridin-1-yl]-3-oxo-propyl}-4-methyl-benzenesulfonamide
CAS NO:90362-80-4
Molecular Formula:
Molecular Weight: 464.626
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-{3-[2-(2,2-Diethoxy-ethyl)-6-prop-(Z)-ylidene-3,6-dihydro-2H-pyridin-1-yl]-3-oxo-propyl}-4-methyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-{3-[2-(2,2-Diethoxy-ethyl)-6-prop-(Z)-ylidene-3,6-dihydro-2H-pyridin-1-yl]-3-oxo-propyl}-4-methyl-benzenesulfonamide(90362-80-4)
EPA Substance Registry System: N-{3-[2-(2,2-Diethoxy-ethyl)-6-prop-(Z)-ylidene-3,6-dihydro-2H-pyridin-1-yl]-3-oxo-propyl}-4-methyl-benzenesulfonamide(90362-80-4)

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: 90362-80-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90362-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,6 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90362-80:
(7*9)+(6*0)+(5*3)+(4*6)+(3*2)+(2*8)+(1*0)=124
124 % 10 = 4
So 90362-80-4 is a valid CAS Registry Number.

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90362-80-4Relevant academic research and scientific papers

SYNTHESIS OF A COMPOUND HAVING A PALUSTRINE STRUCTURE

Natsume, Mitsutaka,Ogawa, Masashi,Yoda, Izumi,Shiro, Motoo

, p. 812 - 814 (2007/10/02)

Total synthesis of the compound (1) having the proposed structure for the horsetail alkaloid palustrine was achieved stereoselectively in a racemic form.The synthesized compoun (1), whose structure was proved by X-ray analysis, was not identical with palu

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