78104-88-8 Usage
Explanation
Different sources of media describe the Explanation of 78104-88-8 differently. You can refer to the following data:
1. 1-methylcyclopropane-1-carbonitrile consists of 5 carbon atoms, 7 hydrogen atoms, and 1 nitrogen atom.
2. The compound appears as a colorless liquid under normal conditions.
3. 1-methylcyclopropane-1-carbonitrile has an unpleasant, strong smell.
4. It serves as a starting material or intermediate in the production of various drugs and pesticides.
5. It can dissolve certain polymers, making it useful in various chemical processes and industries.
6. 1-methylcyclopropane-1-carbonitrile can be used as a reactant in organic chemical reactions to form new compounds.
7. Insecticidal properties
7. The compound has been shown to be effective in killing or repelling insects, leading to its use in insecticide production.
8. 1-methylcyclopropane-1-carbonitrile can easily catch fire and burn, requiring careful handling and storage.
9. Inhaling the vapors of 1-methylcyclopropane-1-carbonitrile can cause irritation and discomfort in the respiratory system.
Physical state
Colorless liquid
Odor
Sharp, pungent
Usage
Different sources of media describe the Usage of 78104-88-8 differently. You can refer to the following data:
1. Precursor in synthesis of pharmaceuticals and agrochemicals
2. Solvent for polymers
3. Reagent in organic synthesis
Flammability
Highly flammable
Health hazard
Respiratory irritation
Check Digit Verification of cas no
The CAS Registry Mumber 78104-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,0 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78104-88:
(7*7)+(6*8)+(5*1)+(4*0)+(3*4)+(2*8)+(1*8)=138
138 % 10 = 8
So 78104-88-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H7N/c1-5(4-6)2-3-5/h2-3H2,1H3
78104-88-8Relevant articles and documents
A process for preparing 1-methyl propyl formic acid method
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Paragraph 0038; 0039, (2017/02/09)
The invention discloses a method for preparing 1-methyl cyclopropane carboxylic acid and belongs to the fields of fine chemical engineering and medical intermediates. The method comprises the following steps: by taking methacrylic acid (ester or salt), or methacrylonitrile or methacrylamide as a raw material, carrying out a cyclopropanation reaction with trihalide in the presence of an alkali to generate 2,2-geminal halide (III); carrying out a reaction between the 2,2-geminal halide (III) and metallic sodium to remove halogen atoms on the ring so as to generate methyl cyclopropionate or methyl cyclopropaneacetonitrile or methyl cyclopropylamide (II); acidifying the methyl cyclopropanecarboxylate, thereby obtaining 1-methyl cyclopropane carboxylic acid (I); and performing basic hydrolysis on methyl cyclopropaneacetonitrile or methyl cyclopropylamide, and acidifying to obtain 1-methyl cyclopropane carboxylic acid (I). The method disclosed by the invention is readily available in raw materials, mild in reaction conditions, convenient to operate, low in cost and high in purity of the obtained product and is a feasible preparation method.
CYCLOAMINO DERIVATIVES AS GPR119 ANTAGONISTS
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Page/Page column 104, (2011/12/14)
Therapeutic compounds are disclosed having the general formula (I) that are useful for the treatment of metabolic disorders, including type II diabetes. The compounds have activity as agonists of GPR119. Compounds having the stereochemistry of formula (la) may also demonstrate DPP-IV inhibitory activity.
PHOTOELECTRON SPECTRA AND MOLECULAR ORBITALS OF 1-METHYL-1-CYANOCYLOPROPANE AND 3-METHYL-3-CYANOCYCLOPROPENE
Plemenkov, V. V.,Redchenko, V. V.,Ermolaeva, L.V.,Bolesov, I. G.,Gritsenko, E. I.
, p. 184 - 187 (2007/10/02)
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