Cas 186308-22-5,[5-cyano-3,4-bis-(2-methoxy-ethoxymethoxy)-thiophen-2-yl]-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid benzhydryl ester

186308-22-5

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Basic information

Product Name: [5-cyano-3,4-bis-(2-methoxy-ethoxymethoxy)-thiophen-2-yl]-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid benzhydryl ester
Synonyms: [5-cyano-3,4-bis-(2-methoxy-ethoxymethoxy)-thiophen-2-yl]-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid benzhydryl ester
CAS NO:186308-22-5
Molecular Formula:
Molecular Weight: 702.739
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: [5-cyano-3,4-bis-(2-methoxy-ethoxymethoxy)-thiophen-2-yl]-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid benzhydryl ester(CAS DataBase Reference)
NIST Chemistry Reference: [5-cyano-3,4-bis-(2-methoxy-ethoxymethoxy)-thiophen-2-yl]-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid benzhydryl ester(186308-22-5)
EPA Substance Registry System: [5-cyano-3,4-bis-(2-methoxy-ethoxymethoxy)-thiophen-2-yl]-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid benzhydryl ester(186308-22-5)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 186308-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 186308-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,3,0 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 186308-22:
(8*1)+(7*8)+(6*6)+(5*3)+(4*0)+(3*8)+(2*2)+(1*2)=145
145 % 10 = 5
So 186308-22-5 is a valid CAS Registry Number.

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186308-22-5Relevant academic research and scientific papers

Synthesis of a dihydroxythiophene analogue of catechosporines

Dini,Aszodi

, p. 349 - 352 (2000)

A vinylogous cephalosporine bearing a dihydroxythiophene moiety as a potential catechol surrogate has been synthesised (I-e-β). Even if the anti staphylococcus spectrum displayed by this compound is of interest, its activity against Pseudomonas species, expected for such a structure, remains disappointing. (C) 2000 Elsevier Science Ltd. All rights reserved.

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