Cas 95668-01-2,1-oxo-1,2,3,12-tetrahydro-thiopyrano<3,2-c>thiopyrano<3,2-c><1,2>benzooxathiin 5,5-dioxide

95668-01-2

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Basic information

Product Name: 1-oxo-1,2,3,12-tetrahydro-thiopyrano<3,2-c>thiopyrano<3,2-c><1,2>benzooxathiin 5,5-dioxide
Synonyms: 1-oxo-1,2,3,12-tetrahydro-thiopyrano<3,2-c>thiopyrano<3,2-c><1,2>benzooxathiin 5,5-dioxide
CAS NO:95668-01-2
Molecular Formula:
Molecular Weight: 338.429
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-oxo-1,2,3,12-tetrahydro-thiopyrano<3,2-c>thiopyrano<3,2-c><1,2>benzooxathiin 5,5-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: 1-oxo-1,2,3,12-tetrahydro-thiopyrano<3,2-c>thiopyrano<3,2-c><1,2>benzooxathiin 5,5-dioxide(95668-01-2)
EPA Substance Registry System: 1-oxo-1,2,3,12-tetrahydro-thiopyrano<3,2-c>thiopyrano<3,2-c><1,2>benzooxathiin 5,5-dioxide(95668-01-2)

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: 95668-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95668-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,6 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95668-01:
(7*9)+(6*5)+(5*6)+(4*6)+(3*8)+(2*0)+(1*1)=172
172 % 10 = 2
So 95668-01-2 is a valid CAS Registry Number.

95668-01-2Upstream product

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95668-01-2Relevant academic research and scientific papers

NEW HETEROCYCLIC RING SYSTEMS. XIV. 7,11-DITHIAOXASTEROIDS ANALOGUES

Cecchetti, Violetta,Fravolini, Arnaldo,Fringuelli, Renata,Schiaffella, Fausto

, p. 2293 - 2300 (2007/10/02)

By reaction of 1,2-benzooxathiin-4(3H)-one 2,2-dioxide (II) with mercaptopropionic acid the new tricycle 4-oxo-3,4-dihydro-2H-thiopyranobenzooxathiin 5,5-dioxide (IV) together with tetracycle V and pentacycle VII were obtained.The key ketone IV was then converted to β-diketone IX, enamino ketone XVI and α-bromoketone XX intermediates to give with nucleophilic reagents 7,11-dithiaoxasteroids analogues.

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