Cas 76557-59-0,1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-ene-3,4-dione 4-(N-phenylthiosemicarbazone)

76557-59-0

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Basic information

Product Name: 1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-ene-3,4-dione 4-(N-phenylthiosemicarbazone)
Synonyms: 1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-ene-3,4-dione 4-(N-phenylthiosemicarbazone)
CAS NO:76557-59-0
Molecular Formula: C₂₅H₃₃N₃O₂S
Molecular Weight: 439.61342
EINECS: N/A
Product Categories: N/A
Mol File: 76557-59-0.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-ene-3,4-dione 4-(N-phenylthiosemicarbazone)(CAS DataBase Reference)
NIST Chemistry Reference: 1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-ene-3,4-dione 4-(N-phenylthiosemicarbazone)(76557-59-0)
EPA Substance Registry System: 1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-ene-3,4-dione 4-(N-phenylthiosemicarbazone)(76557-59-0)

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: 76557-59-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76557-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,5 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76557-59:
(7*7)+(6*6)+(5*5)+(4*5)+(3*7)+(2*5)+(1*9)=170
170 % 10 = 0
So 76557-59-0 is a valid CAS Registry Number.

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76557-59-0Relevant academic research and scientific papers

Di-isophorone and Related Compounds. Part 6. The Action of Nucleophiles on 8-Bromodi-isophorone

Davies, Paul R.,Kurzer, Frederick,Morgan, Alan R.

, p. 1097 - 1110 (2007/10/02)

Hydrolysis and acetolysis of 8-bromo-1-hydroxydi-isophor-2(7)-en-3-one yields both epimeric forms of the corresponding 4-hydroxy and 4-acetoxy compounds, probably by a mechanism involving a bimolecular (SN2'') displacement.The action of excess of hydrazin

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