Cas 89880-34-2,Cyclohexanone, 2-[1-hydroxy-1-methyl-2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-

89880-34-2

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Basic information

Product Name: Cyclohexanone, 2-[1-hydroxy-1-methyl-2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-
Synonyms:
CAS NO:89880-34-2
Molecular Formula: C14H24O4
Molecular Weight: 256.342
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: Cyclohexanone, 2-[1-hydroxy-1-methyl-2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Cyclohexanone, 2-[1-hydroxy-1-methyl-2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-(89880-34-2)
EPA Substance Registry System: Cyclohexanone, 2-[1-hydroxy-1-methyl-2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-(89880-34-2)

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: 89880-34-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89880-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,8 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89880-34:
(7*8)+(6*9)+(5*8)+(4*8)+(3*0)+(2*3)+(1*4)=192
192 % 10 = 2
So 89880-34-2 is a valid CAS Registry Number.

89880-34-2Upstream product

89880-34-2Downstream Products

1919-00-2 4,5,6,7-tetrahydro-3-methylbenzofuran

89880-34-2Relevant academic research and scientific papers

New Route for Synthesis of Furan Derivatives from Protected α-Ketols and Ketones. A Total Synthesis of Furoventalene

Hagiwara, Hisahiro,Uda, Hisashi

, p. 91 - 94 (2007/10/02)

Reaction of acetonyl tetrahydropyranyl ether (1) with ketones (2a-d) in the presence of lithium di-isopropylamide and zinc chloride produces the cross-aldol condensation products (3a-d), which are transformed into 3-methylfurans (4a-d), by treatment with

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