Cas 159788-96-2,1,19-dimethyl-22-phenyl-4,7,10,13,16-pentaoxa-25-thia-22-azatetracyclo<17.5.1.0<sup>2,18</sup>.0<sup>20,24</sup>>pentacosa-2(18)-ene-21,23-dione 25-oxide

159788-96-2

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Product Name: 1,19-dimethyl-22-phenyl-4,7,10,13,16-pentaoxa-25-thia-22-azatetracyclo<17.5.1.0^2,18.0^20,24>pentacosa-2(18)-ene-21,23-dione 25-oxide
Synonyms:
CAS NO:159788-96-2
Molecular Formula:
Molecular Weight: 519.616
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: 1,19-dimethyl-22-phenyl-4,7,10,13,16-pentaoxa-25-thia-22-azatetracyclo<17.5.1.0^2,18.0^20,24>pentacosa-2(18)-ene-21,23-dione 25-oxide(CAS DataBase Reference)
NIST Chemistry Reference: 1,19-dimethyl-22-phenyl-4,7,10,13,16-pentaoxa-25-thia-22-azatetracyclo<17.5.1.0^2,18.0^20,24>pentacosa-2(18)-ene-21,23-dione 25-oxide(159788-96-2)
EPA Substance Registry System: 1,19-dimethyl-22-phenyl-4,7,10,13,16-pentaoxa-25-thia-22-azatetracyclo<17.5.1.0^2,18.0^20,24>pentacosa-2(18)-ene-21,23-dione 25-oxide(159788-96-2)

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: 159788-96-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 159788-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,7,8 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 159788-96:
(8*1)+(7*5)+(6*9)+(5*7)+(4*8)+(3*8)+(2*9)+(1*6)=212
212 % 10 = 2
So 159788-96-2 is a valid CAS Registry Number.

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159788-96-2Relevant academic research and scientific papers

Novel Crown Ethers by Oxidative Cycloaddition of Thiopheno Crown Ethers

Li, YuanQiang,Thiemann, Thies,Sawada, Tsuyoshi,Tashiro, Masashi

, p. 2323 - 2330 (2007/10/02)

The synthesis of the thiopheno crown ethers 4 is described.The oxidative cycloaddition of these and the known thiopheno crown ethers 2 with N-phenylmaleimide is reported.The resulting sulfoxy-bridged cycloadducts 15 and 16 are transformed oxidatively into

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