Cas 81924-65-4,(3S,3aS,6S,9bS)-6-Hydroxy-3,6,9-trimethyl-3a,5,6,9b-tetrahydro-3H,4H-1,8-dioxa-cyclopenta[e]azulen-2-one

81924-65-4

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Basic information

Product Name: (3S,3aS,6S,9bS)-6-Hydroxy-3,6,9-trimethyl-3a,5,6,9b-tetrahydro-3H,4H-1,8-dioxa-cyclopenta[e]azulen-2-one
Synonyms:
CAS NO:81924-65-4
Molecular Formula:
Molecular Weight: 250.295
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: (3S,3aS,6S,9bS)-6-Hydroxy-3,6,9-trimethyl-3a,5,6,9b-tetrahydro-3H,4H-1,8-dioxa-cyclopenta[e]azulen-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,3aS,6S,9bS)-6-Hydroxy-3,6,9-trimethyl-3a,5,6,9b-tetrahydro-3H,4H-1,8-dioxa-cyclopenta[e]azulen-2-one(81924-65-4)
EPA Substance Registry System: (3S,3aS,6S,9bS)-6-Hydroxy-3,6,9-trimethyl-3a,5,6,9b-tetrahydro-3H,4H-1,8-dioxa-cyclopenta[e]azulen-2-one(81924-65-4)

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: 81924-65-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81924-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,2 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81924-65:
(7*8)+(6*1)+(5*9)+(4*2)+(3*4)+(2*6)+(1*5)=144
144 % 10 = 4
So 81924-65-4 is a valid CAS Registry Number.

81924-65-4Upstream product

24399-20-0 artabsin

81924-65-4Downstream Products

81924-65-4Relevant academic research and scientific papers

Structures of the Artabsinolides; Photo-oxygenation Studies on Artabsin

Beauhaire, Josiane,Fourrey, Jean-Louis

, p. 861 - 864 (2007/10/02)

The structure and stereochemistry of four new guaianolides from Artemisia absinthium, named artabsinolides A, B, C, and D, have been established.They were synthesized via rearrangement or reduction of the endo-peroxides resulting from dye-sensitized photo-oxygenation of the main constituent of the plant, artabsin (1).

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