Cas 1198176-79-2,1,3,11,13-tetramethoxy-2,12-dibenzyloxy-8-methyl-8-hydroxy-5,7,9-trihydro-7H-dibenzo[a,c]cyclononen-6-one

1198176-79-2

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Basic information

Product Name: 1,3,11,13-tetramethoxy-2,12-dibenzyloxy-8-methyl-8-hydroxy-5,7,9-trihydro-7H-dibenzo[a,c]cyclononen-6-one
Synonyms: 1,3,11,13-tetramethoxy-2,12-dibenzyloxy-8-methyl-8-hydroxy-5,7,9-trihydro-7H-dibenzo[a,c]cyclononen-6-one
CAS NO:1198176-79-2
Molecular Formula:
Molecular Weight: 598.693
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: 1,3,11,13-tetramethoxy-2,12-dibenzyloxy-8-methyl-8-hydroxy-5,7,9-trihydro-7H-dibenzo[a,c]cyclononen-6-one(CAS DataBase Reference)
NIST Chemistry Reference: 1,3,11,13-tetramethoxy-2,12-dibenzyloxy-8-methyl-8-hydroxy-5,7,9-trihydro-7H-dibenzo[a,c]cyclononen-6-one(1198176-79-2)
EPA Substance Registry System: 1,3,11,13-tetramethoxy-2,12-dibenzyloxy-8-methyl-8-hydroxy-5,7,9-trihydro-7H-dibenzo[a,c]cyclononen-6-one(1198176-79-2)

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: 1198176-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1198176-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,1,7 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1198176-79:
(9*1)+(8*1)+(7*9)+(6*8)+(5*1)+(4*7)+(3*6)+(2*7)+(1*9)=202
202 % 10 = 2
So 1198176-79-2 is a valid CAS Registry Number.

1198176-79-2Upstream product

1198076-86-6 1-[4,6,2',4'-tetramethoxy-5,3'-dibenzyloxy-6'-(2-oxopropyl)biphenyl-2-yl]propan-2-one

1198176-79-2Downstream Products

1198176-79-2Relevant academic research and scientific papers

Synthesis of the cores of hypocrellin and shiraiachrome: diastereoselective 1,8-diketone aldol cyclization

O'Brien, Erin M.,Li, Jingxian,Carroll, Patrick J.,Kozlowski, Marisa C.

experimental part, p. 69 - 73 (2010/04/24)

(Chemical Equation Presented) Intramolecular 1,8-diketone aldol reactions were studied as a tool for the construction of the seven-membered rings of hypocrellin and shiraiachrome. Conditions were identified to obtain the relative stereochemistries present

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