Cas 80714-63-2,3'-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-3,3,5',5',6,6-hexamethyl-3,4,5,6-tetrahydroxanthen-9-spirocyclohex-2'-ene-1(2H),8(7H)-dione

80714-63-2

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Basic information

Product Name: 3'-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-3,3,5',5',6,6-hexamethyl-3,4,5,6-tetrahydroxanthen-9-spirocyclohex-2'-ene-1(2H),8(7H)-dione
Synonyms:
CAS NO:80714-63-2
Molecular Formula:
Molecular Weight: 506.682
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'-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-3,3,5',5',6,6-hexamethyl-3,4,5,6-tetrahydroxanthen-9-spirocyclohex-2'-ene-1(2H),8(7H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 3'-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-3,3,5',5',6,6-hexamethyl-3,4,5,6-tetrahydroxanthen-9-spirocyclohex-2'-ene-1(2H),8(7H)-dione(80714-63-2)
EPA Substance Registry System: 3'-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-3,3,5',5',6,6-hexamethyl-3,4,5,6-tetrahydroxanthen-9-spirocyclohex-2'-ene-1(2H),8(7H)-dione(80714-63-2)

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: 80714-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80714-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,1 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80714-63:
(7*8)+(6*0)+(5*7)+(4*1)+(3*4)+(2*6)+(1*3)=122
122 % 10 = 2
So 80714-63-2 is a valid CAS Registry Number.

80714-63-2Upstream product

3471-13-4 dimedone

80714-63-2Downstream Products

80714-63-2Relevant academic research and scientific papers

Reactions between Enaminones and Enones. Part 2. C versus N-Alkylation with Cyclohex-2-enone. Structure Confirmation by Reduction of a Dienaminone Derivative of Dehydrated Dimedone Dimer

Chaaban, Ibrahim,Greenhill, John V.,Ramli, Mohamed

, p. 3120 - 3124 (2007/10/02)

Primary and secondary enaminones derived from cyclohexane-1,3-dione, dimedone, and acetylacetone react with cyclohexenone to give exclusively C-alkylated derivatives.In every case the products form carbinolamines which exist as 1-hydroxy-2-azacyclo

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