62199-50-2 Usage
Class
Cyclopentane derivatives
This compound belongs to a group of organic compounds that contain a cyclopentane ring structure in their molecular structure.
Structural components
Butyl group, Propyl group
1α-Butyl-2β-propylcyclopentane is composed of a butyl group (four-carbon chain) and a propyl group (three-carbon chain) attached to the cyclopentane ring.
Usage
Synthetic intermediate
This chemical is commonly used as a building block or intermediate in the synthesis of various industrial and consumer products.
Potential applications
Pharmaceuticals, Agrochemicals
Due to its structural properties and reactivity, 1α-Butyl-2β-propylcyclopentane may have potential applications in the fields of pharmaceuticals and agrochemicals.
Versatility
Organic synthesis building block
As a versatile building block, 1α-Butyl-2β-propylcyclopentane can be used to synthesize a wide range of diverse organic compounds, making it valuable in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 62199-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,9 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62199-50:
(7*6)+(6*2)+(5*1)+(4*9)+(3*9)+(2*5)+(1*0)=132
132 % 10 = 2
So 62199-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H24/c1-3-5-8-12-10-6-9-11(12)7-4-2/h11-12H,3-10H2,1-2H3
62199-50-2Relevant articles and documents
Open-chain and Cyclic Bis-phosphoranes from α,ω-Dinitriles, Diisobutylaluminium Hydride, and Methylenetriphenylphosphorane
Bogdanovic, Borislav,Hullen, Albert,Konstantinovic, Stanimir,Krawiecka, Bozena,Mynott, Richard
, p. 2261 - 2271 (2007/10/02)
The reaction of subero-, azelao-, and sebaconitrile (4, n = 6, 7, and 8) with diisobutylaluminium hydride (to give 5) and subsequenly with methylenetriphenylphosphorane leads to the openc-hain bis-phosphoranes 8 a-c, which have been characterized by the Wittig reaction.The same reaction sequence applied to adiponitrile produces the cyclic bis-phosphorane 9a.The previously unknown hydrocarbon 1,3,9,11-cyclohexadecatetraene (12) has been prepared from 8a and adipoaldehyde.
