50421-83-5 Usage
Cyclic ketone
It is a cyclic ketone, which means it has a ring structure with a carbonyl group (C=O) attached to the ring.
Hydroxymethylene group
It has a hydroxymethylene group (-CHOH-), which is a functional group consisting of a carbon atom double-bonded to an oxygen atom and single-bonded to a hydrogen atom and a hydroxyl group (-OH).
Isopropyl side chain
It has an isopropyl side chain (-CH(CH3)2), which is a functional group consisting of a carbon atom bonded to three hydrogen atoms and to an -Ogroup.
Industrial uses
2-(hydroxymethylene)-6-(isopropyl)-3-methylcyclohexan-1-one is used in various industrial processes and as a building block for the synthesis of other organic compounds.
Applications
It has a range of applications in the production of pharmaceuticals, fragrances, and flavors.
Unique structure and chemical properties
Its unique structure and chemical properties make it a valuable intermediate in organic chemistry and a subject of interest for researchers in the field.
Check Digit Verification of cas no
The CAS Registry Mumber 50421-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,2 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50421-83:
(7*5)+(6*0)+(5*4)+(4*2)+(3*1)+(2*8)+(1*3)=85
85 % 10 = 5
So 50421-83-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O2/c1-7(2)9-5-4-8(3)10(6-12)11(9)13/h6-9,12H,4-5H2,1-3H3/b10-6-
50421-83-5Relevant academic research and scientific papers
New optically active pyrazoles: Syntheses and the structural characterization of menthopyrazole analogues
Kashima, Choji,Miwa, Yohei,Shibata, Saori,Nakazono, Hiroyuki
, p. 1235 - 1240 (2007/10/03)
New chiral pyrazoles, (4R,7R)-4-methyl-7-isopropyl-3-phenyl- (3-phenylisomenthopyrazole; cis-1), (4R,7S)-4-methyl-7-isopropyl- (l-menthopyrazole; trans-2), (4R,7R)-4-isopropyl-7-methyl- (isocarvomenthopyrazole, cis-3) and (4R,7S)-4-isopropyl-7-methyl-4,5,6,7-tetrahydro-1H-indazole (carvomenthopyrazole, trans-3) were prepared. The diastereomeric pairs of these 1-3 were structurally characterized by NMR spectroscopy. The subtle differences of structures of 1-3 should induce the useful effects for a chiral auxiliary or a chiral catalyst.
