116111-72-9 Usage
Explanation
The compound's full name, which describes its structure and composition.
Explanation
The primary applications of the compound in various industries.
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The compound's appearance and state of matter at room temperature.
Explanation
The characteristic scent of the compound.
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The compound's tendency to catch fire or burn easily.
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The compound's role in the creation of various medications.
Explanation
The compound's use in the formation of different organic substances.
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The compound's function as a solvent for extracting components from natural sources.
Explanation
The compound's role in providing stability to a range of products.
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The compound's classification as a substance that may cause harm to the environment if not managed properly.
Explanation
The potential negative impact on human health if the compound is not handled or used correctly.
Common Uses
Solvent, reagent in chemical reactions
Physical State
Clear, colorless liquid
Odor
Faint sweet smell
Flammability
Highly flammable
Applications in Pharmaceutical Industry
Production of pharmaceuticals
Synthesis
Organic compounds
Solvent in Extraction
Natural products
Stabilizer
Formulation of various products
Environmental Hazard
Potential environmental hazard
Health Risks
Adverse effects on human health
Check Digit Verification of cas no
The CAS Registry Mumber 116111-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,1 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116111-72:
(8*1)+(7*1)+(6*6)+(5*1)+(4*1)+(3*1)+(2*7)+(1*2)=79
79 % 10 = 9
So 116111-72-9 is a valid CAS Registry Number.
116111-72-9Relevant academic research and scientific papers
Oxime ethers, the preparation thereof, compositions containing them and use thereof
-
, (2008/06/13)
The invention relates to oxime ethers of the formula I STR1 wherein n is 1 or 2, each of R1 and R2 is hydrogen or C1 -C4 alkyl each of R3 and R4 is hydrogen, halogen, C1 -C4 alkyl, C1 -C4 haloalkyl, C1 -C4 alkoxy, C1 -C4 haloalkoxy, C1 -C4 alkylthio, C1 -C4 haloalkylthio, C1 -C4 alkylsulfinyl, C1 -C4 alkylsulfonyl, C1 -C4 haloalkylsulfinyl, C1 -C4 haloalkylsulfonyl or nitro; each of R5 and R6 independently of the other is hydrogen, C1 -C4 alkyl, C1 -C4 haloalkyl, phenyl or phenyl which is substituted by halogen, C1 -C4 alkyl, C1 -C4 haloalkyl, C1 -C4 alkoxy, C1 -C4 haloalkoxy, C1 -C4 alkylthio, C1 -C4 alkylsulfinyl, C1 -C4 alkylsulfonyl, carboxyl, carbamoyl, C 1 -C4 alkylcarbamoyl, nitro or cyano, or R5 and R6 together are also a 2- to 6-membered alkylene or alkenylene chain which may be substituted by C1 -C4 alkyl radicals; X is hydrogen, cyano, nitro, chlorine, C1 -C4 alkyl, C1 -C4 haloalkyl, C3 -C6 cycloalkyl, carboxyl, carbamoyl, C1 -C4 alkylcarbonyl, C1 -C4 alkoxycarbonyl or C1 -C4 alkylcarbamoyl. The oxime ethers of the formula I are able to act as antidotes or safeners to protect cultivated plants from the phytotoxic effects of herbicides. Such cultivated plants are preferably sorghum, cereals, maize and rice.
Fragmentation of Cyclic Carboxonium Ions, IV. - Synthesis of β-Oxa-γ, δ-enones
Mattay, Jochen,Thuenker, Walter,Scharf, Hans-Dieter
, p. 1105 - 1117 (2007/10/02)
The proton-catalyzed fragmentation of 4-methylene-1,3-dioxolanes 2 by weak acids (pK > 4.3) or weak acidic ion exchangers leads in good yields to β-oxa-γ, δ-enones 5 which are thus easily and generally available for the first time.
