Cas 77587-23-6,Formic acid (E)-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-6-(2-oxo-1,2-dihydro-quinolin-4-yloxy)-hex-4-enyl ester

77587-23-6

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Basic information

Product Name: Formic acid (E)-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-6-(2-oxo-1,2-dihydro-quinolin-4-yloxy)-hex-4-enyl ester
Synonyms: Formic acid (E)-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-6-(2-oxo-1,2-dihydro-quinolin-4-yloxy)-hex-4-enyl ester
CAS NO:77587-23-6
Molecular Formula:
Molecular Weight: 359.422
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: Formic acid (E)-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-6-(2-oxo-1,2-dihydro-quinolin-4-yloxy)-hex-4-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Formic acid (E)-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-6-(2-oxo-1,2-dihydro-quinolin-4-yloxy)-hex-4-enyl ester(77587-23-6)
EPA Substance Registry System: Formic acid (E)-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-6-(2-oxo-1,2-dihydro-quinolin-4-yloxy)-hex-4-enyl ester(77587-23-6)

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: 77587-23-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 77587-23-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,8 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77587-23:
(7*7)+(6*7)+(5*5)+(4*8)+(3*7)+(2*2)+(1*3)=176
176 % 10 = 6
So 77587-23-6 is a valid CAS Registry Number.

77587-23-6Upstream product

5389-87-7 1-chloro-3,7-dimethylocta-2,6-diene

77587-23-6Downstream Products

21059-47-2 bucharaine

77587-23-6Relevant academic research and scientific papers

Quinoline Alkaloids. Part 22. Synthesis of the Monoterpenoid Quinoline Alkaloid, Bucharaine

Grundon Michael F.,Ramachandran, V. N.,Donnelly, Michael E.

, p. 633 - 635 (2007/10/02)

Reaction of 4-hydroxy-2-quinolone with geranyl chloride gave the geranyl ether (5a), the C-geranyl derivatives (6) and (7), and the vinylhexenyl derivative (8).The geranyl ether was converted into bucharaine (1) by selective hydroxylation and via mono-epoxydation.

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