18450-74-3 Usage
Uses
Used in Pharmaceutical Industry:
(2S,4R)-(-)-2,4-dimethylheptan-1-ol is used as a chiral building block for the synthesis of various pharmaceuticals, leveraging its unique stereochemistry to create enantiomerically pure compounds with targeted therapeutic effects.
Used in Flavor and Fragrance Industry:
(2S,4R)-(-)-2,4-dimethylheptan-1-ol is utilized as a chiral building block in the creation of flavors and fragrances, contributing to the development of novel scents and tastes with enhanced purity and specificity.
Used in Antimicrobial Applications:
(2S,4R)-(-)-2,4-dimethylheptan-1-ol has been studied for its potential antimicrobial properties, making it a candidate for use in applications requiring the inhibition of microbial growth, such as in the development of preservatives or disinfectants.
Used in Anti-inflammatory Applications:
(2S,4R)-(-)-2,4-dimethylheptan-1-ol has also been investigated for its anti-inflammatory properties, suggesting potential use in the development of treatments for conditions characterized by inflammation, such as arthritis or dermatitis.
Check Digit Verification of cas no
The CAS Registry Mumber 18450-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,5 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18450-74:
(7*1)+(6*8)+(5*4)+(4*5)+(3*0)+(2*7)+(1*4)=113
113 % 10 = 3
So 18450-74-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O/c1-4-5-8(2)6-9(3)7-10/h8-10H,4-7H2,1-3H3/t8-,9+/m1/s1
18450-74-3Relevant academic research and scientific papers
Synthesis of (2R,4R)-supellapyrone, the sex pheromone of the brownbanded cockroach, Supella longipalpa, and its three stereoisomers
Fujita, Ken,Mori, Kenji
, p. 493 - 502 (2007/10/03)
Supellapyrone [(2R,4R)-5-(2,4-dimethyl)-3-methyl-2H-pyran-2-one (1)], the female sex pheromone of the brownbanded cockroach (Supella longipalpa), and its three stereoisomers were synthesized by employing lipase-catalyzed desymmetrization or enantiomer separation of syn- or anti-2,4-dimethylpentane-1,5-diol (9) as the key step.
STEREOCHEMISTRY OF LARDOLURE. THE AGGREGATION PHEROMONE OF THE ACARID MITE, LARDOGLYPHUS KONOI
Mori, Kenji,Kuwahara, Shigefumi
, p. 5545 - 5550 (2007/10/02)
(1R,3R,5R,7R)-Stereochemistry was assigned to lardolure (1,3,5,7-tetramethyldecyl formate) on the basis of GLC comparison of the natural pheromone with the synthetic pheromones prepared in partially stereocontrolled manners.
