Cas 1027191-56-5,Methanesulfonic acid 4-methanesulfonyloxy-2-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-butyl ester

1027191-56-5

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Basic information

Product Name: Methanesulfonic acid 4-methanesulfonyloxy-2-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-butyl ester
Synonyms: Methanesulfonic acid 4-methanesulfonyloxy-2-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-butyl ester
CAS NO:1027191-56-5
Molecular Formula:
Molecular Weight: 364.441
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: Methanesulfonic acid 4-methanesulfonyloxy-2-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methanesulfonic acid 4-methanesulfonyloxy-2-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-butyl ester(1027191-56-5)
EPA Substance Registry System: Methanesulfonic acid 4-methanesulfonyloxy-2-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-butyl ester(1027191-56-5)

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: 1027191-56-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027191-56-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,1,9 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1027191-56:
(9*1)+(8*0)+(7*2)+(6*7)+(5*1)+(4*9)+(3*1)+(2*5)+(1*6)=125
125 % 10 = 5
So 1027191-56-5 is a valid CAS Registry Number.

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1027191-56-5Relevant academic research and scientific papers

A new class of potential chloroquine-resistance reversal agents for plasmodia: Syntheses and biological evaluation of 1-(3'-Diethylaminopropyl)-3-(substituted phenylmethylene)pyrrolidines

Batra,Srivastava,Roy,Pandey,Bhaduri

, p. 3428 - 3433 (2000)

1-(3'-Diethylaminopropyl)-3-(substituted phenylmethylene)pyrrolidines were synthesized and evaluated for CQ-resistant reversal activity. In general the compounds of the series elicit better biological response than their phenylmethyl analogues. The most a

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