Cas 92693-84-0,3-<(N-methylphenylsulphonimidoyl)methyl>-exo-2-<7-(tetrahydropyran-2-yloxy)heptyl>-8-oxabicyclo<3.2.1>octan-3-ol

92693-84-0

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Basic information

Product Name: 3-<(N-methylphenylsulphonimidoyl)methyl>-exo-2-<7-(tetrahydropyran-2-yloxy)heptyl>-8-oxabicyclo<3.2.1>octan-3-ol
Synonyms:
CAS NO:92693-84-0
Molecular Formula:
Molecular Weight: 493.708
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: 3-<(N-methylphenylsulphonimidoyl)methyl>-exo-2-<7-(tetrahydropyran-2-yloxy)heptyl>-8-oxabicyclo<3.2.1>octan-3-ol(CAS DataBase Reference)
NIST Chemistry Reference: 3-<(N-methylphenylsulphonimidoyl)methyl>-exo-2-<7-(tetrahydropyran-2-yloxy)heptyl>-8-oxabicyclo<3.2.1>octan-3-ol(92693-84-0)
EPA Substance Registry System: 3-<(N-methylphenylsulphonimidoyl)methyl>-exo-2-<7-(tetrahydropyran-2-yloxy)heptyl>-8-oxabicyclo<3.2.1>octan-3-ol(92693-84-0)

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: 92693-84-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 92693-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,9 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92693-84:
(7*9)+(6*2)+(5*6)+(4*9)+(3*3)+(2*8)+(1*4)=170
170 % 10 = 0
So 92693-84-0 is a valid CAS Registry Number.

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92693-84-0Relevant academic research and scientific papers

The Synthesis of (+/-)-10a-Homo-11a-carbathromboxane A1, a Stable Thromboxane A Analogue

Ansell, Martin F.,Mason, Jonathan S.,Caton, Michael P. L.

, p. 1061 - 1068 (1984)

The thromboxane A1 (TXA1) analogue (1), which retains the characteristic bridge oxygen atom of the TXA molecule, has been synthesized from the bicyclic ketone (2).Stereochemical control of alkylation of the bicyclic ketone (2) was ac

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