3422-07-9 Usage
Cyclopropane derivative
It is a modified version of cyclopropane, a three-membered ring structure.
Methyl group attachment
A methyl group (CH3) is attached to one of the carbon atoms in the cyclopropane ring.
Propenyl group attachment
A propenyl group (CH2=CH-CH3) is attached to another carbon atom in the cyclopropane ring.
Physical state at room temperature
1-methyl-1-(prop-1-en-2-yl)cyclopropane is a colorless liquid.
Uses in organic synthesis
It is commonly used as a reagent in organic synthesis and as a building block for the preparation of various organic compounds.
Flammability
The compound is flammable, which means it can easily catch fire or explode when exposed to an ignition source.
Potential hazards
1-methyl-1-(prop-1-en-2-yl)cyclopropane can be hazardous if not handled properly, posing risks to human health and the environment.
Safety precautions
It should be stored and used in a well-ventilated area with appropriate safety measures, such as wearing protective gear and following proper handling guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 3422-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,2 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3422-07:
(6*3)+(5*4)+(4*2)+(3*2)+(2*0)+(1*7)=59
59 % 10 = 9
So 3422-07-9 is a valid CAS Registry Number.
3422-07-9Relevant articles and documents
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Sakai,M. et al.
, p. 4611 - 4613 (1971)
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REACTIONS OF CYCLOPROPENES WITH DIAZOMETHANE IN THE PRESENCE OF PALLADIUM COMPOUNDS
Lukin, K. A.,Zefirov, N. S.
, p. 242 - 246 (2007/10/02)
The reaction of cyclopropenes with diazomethane in the presence of palladium acetate leads to bicyclobutane isomerization products, to olefins containing 1,4-pentadiene fragments, and to the oligomers of cyclopropenes.The predominating reaction path is determined by the degree of substitution of the double bond.
REACTION OF 1,2,2-TRIMETHYLCYCLOPROPANE WITH DIAZOMETHANE IN THE PRESENCE OF PALLADIUM(II) ACETATE
Lukin, K.A.,Zefirov, N.S.
, p. 184 - 185 (2007/10/02)
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