Cas 76567-95-8,3,5-Dinitro-benzoic acid [(1S,9R)-1-hydroxy-5,5,9,11,11-pentamethyl-3-oxo-tricyclo[7.3.1.0<sup>2,7</sup>]tridec-2<sup>(7)</sup>-en-(4Z)-ylidene]-hydrazide

76567-95-8

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Basic information

Product Name: 3,5-Dinitro-benzoic acid [(1S,9R)-1-hydroxy-5,5,9,11,11-pentamethyl-3-oxo-tricyclo[7.3.1.0^2,7]tridec-2⁽⁷⁾-en-(4Z)-ylidene]-hydrazide
Synonyms:
CAS NO:76567-95-8
Molecular Formula:
Molecular Weight: 498.536
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: 3,5-Dinitro-benzoic acid [(1S,9R)-1-hydroxy-5,5,9,11,11-pentamethyl-3-oxo-tricyclo[7.3.1.0^2,7]tridec-2⁽⁷⁾-en-(4Z)-ylidene]-hydrazide(CAS DataBase Reference)
NIST Chemistry Reference: 3,5-Dinitro-benzoic acid [(1S,9R)-1-hydroxy-5,5,9,11,11-pentamethyl-3-oxo-tricyclo[7.3.1.0^2,7]tridec-2⁽⁷⁾-en-(4Z)-ylidene]-hydrazide(76567-95-8)
EPA Substance Registry System: 3,5-Dinitro-benzoic acid [(1S,9R)-1-hydroxy-5,5,9,11,11-pentamethyl-3-oxo-tricyclo[7.3.1.0^2,7]tridec-2⁽⁷⁾-en-(4Z)-ylidene]-hydrazide(76567-95-8)

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: 76567-95-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76567-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,6 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76567-95:
(7*7)+(6*6)+(5*5)+(4*6)+(3*7)+(2*9)+(1*5)=178
178 % 10 = 8
So 76567-95-8 is a valid CAS Registry Number.

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76567-95-8Relevant 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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