Cas 1413765-37-3,3-hydroxy-3-methyl-1,2-dioxaspiro[5.5]undeca-7,10-dien-9-one

1413765-37-3

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Basic information

Product Name: 3-hydroxy-3-methyl-1,2-dioxaspiro[5.5]undeca-7,10-dien-9-one
Synonyms: 3-hydroxy-3-methyl-1,2-dioxaspiro[5.5]undeca-7,10-dien-9-one
CAS NO:1413765-37-3
Molecular Formula:
Molecular Weight: 196.203
EINECS: N/A
Product Categories: N/A
Mol File: 1413765-37-3.mol
Article Data: 2

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-hydroxy-3-methyl-1,2-dioxaspiro[5.5]undeca-7,10-dien-9-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-hydroxy-3-methyl-1,2-dioxaspiro[5.5]undeca-7,10-dien-9-one(1413765-37-3)
EPA Substance Registry System: 3-hydroxy-3-methyl-1,2-dioxaspiro[5.5]undeca-7,10-dien-9-one(1413765-37-3)

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: 1413765-37-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1413765-37-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,3,7,6 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1413765-37:
(9*1)+(8*4)+(7*1)+(6*3)+(5*7)+(4*6)+(3*5)+(2*3)+(1*7)=153
153 % 10 = 3
So 1413765-37-3 is a valid CAS Registry Number.

1413765-37-3Upstream product

5471-51-2 4-(4-hydroxyphenyl)-2-oxobutane

1413765-37-3Downstream Products

1413765-37-3Relevant articles and documents

Total synthesis of natural p -quinol cochinchinenone

Barradas, Silvia,Hernández-Torres, Gloria,Urbano, Antonio,Carre?o, M. Carmen

, p. 5952 - 5955 (2012)

Cochinchinenone has been synthesized in only five steps and four pots and in 58% overall yield from commercially available 2,3-dimethoxy-4-hydroxy- benzaldehyde and OPMB-protected p-hydroxy acetophenone, the key step being the oxone-mediated oxidative dea

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