Cas 52589-24-9,α,ε,4-Trimethyl-2-oxo-3-cyclohexene-1-hexanal

52589-24-9

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Basic information

Product Name: α,ε,4-Trimethyl-2-oxo-3-cyclohexene-1-hexanal
Synonyms: Ptilostemonal;α,ε,4-Trimethyl-2-oxo-3-cyclohexene-1-hexanal
CAS NO:52589-24-9
Molecular Formula: C₁₅H₂₄O₂
Molecular Weight: 236.34986
EINECS: N/A
Product Categories: N/A
Mol File: 52589-24-9.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: α,ε,4-Trimethyl-2-oxo-3-cyclohexene-1-hexanal(CAS DataBase Reference)
NIST Chemistry Reference: α,ε,4-Trimethyl-2-oxo-3-cyclohexene-1-hexanal(52589-24-9)
EPA Substance Registry System: α,ε,4-Trimethyl-2-oxo-3-cyclohexene-1-hexanal(52589-24-9)

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: 52589-24-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 52589-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,8 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52589-24:
(7*5)+(6*2)+(5*5)+(4*8)+(3*9)+(2*2)+(1*4)=139
139 % 10 = 9
So 52589-24-9 is a valid CAS Registry Number.

52589-24-9Upstream product

52589-24-9Downstream Products

52589-23-8 2-methyl-6-(2-oxo-4-methylcyclohex-3-en-1-yl)heptan-1-ol

52589-24-9Relevant academic research and scientific papers

Synthesis of 2-methyl-6-(4-tolyl)hept-1-ene, 2-methyl-6-(2-oxo-4-methylcyclohex-3-en-1-yl)-1-heptanol and 2-methyl-6-(2-oxo-4-methylcyclohex-3-en-1-yl)-1-heptanal

Arora, Ajay K.,Singh, Jaswinder,Sharma, Munisha,Kad

, p. 592 - 594 (2007/10/03)

Sesquiterpenes, 2-methyl-6-(4-tolyl)hept-1-ene (1), 2-methyl-6-(2-oxo-4-methylcyclohex-3-en-1-yl)-1-heptanol (2) and 2-methyl-6-(2-oxo-4-methylcyclohex-3-en-1-yl)-1-heptanal (3) have been synthesized utilising tandemphenylation reduction and Birch reducti

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