41884-28-0 Usage
Uses
Used in Fragrance Industry:
(R)-2-isopropyl-5-methylhexanol is used as a fragrance ingredient for its pleasant, floral scent, adding a desirable aroma to perfumes and other personal care products.
Used in Cosmetics and Household Products:
(R)-2-isopropyl-5-methylhexanol is used as a fragrance ingredient in cosmetics and household products to provide a pleasant scent and enhance the sensory experience of these products.
Used in Hygiene Products:
(R)-2-isopropyl-5-methylhexanol is used as an ingredient in deodorants and other hygiene products due to its antibacterial and antifungal properties, contributing to their effectiveness in maintaining personal cleanliness and odor control.
Used as a Solvent:
(R)-2-isopropyl-5-methylhexanol is used as a solvent in various formulations, taking advantage of its ability to dissolve other substances and facilitate their application.
Used as a Fragrance Fixative:
(R)-2-isopropyl-5-methylhexanol is used as a fragrance fixative to help stabilize and prolong the scent in perfumes and other fragranced products, ensuring a lasting and consistent aroma.
Check Digit Verification of cas no
The CAS Registry Mumber 41884-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,8 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41884-28:
(7*4)+(6*1)+(5*8)+(4*8)+(3*4)+(2*2)+(1*8)=130
130 % 10 = 0
So 41884-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O/c1-8(2)5-6-10(7-11)9(3)4/h8-11H,5-7H2,1-4H3/t10-/m0/s1
41884-28-0Relevant academic research and scientific papers
Suzukamo, Gohfu,Fukao, Masami,Tamura, Mitsuhisa
, p. 1595 - 1598 (1984)
Treatment of alkyl chrysanthemate with Lewis acid leads to C3 epimerization, while protonic acid treatment gives rise to selective C2-C3 bond cleavage.The latter method is succesfully applied to the synthesis of optically active tetrahydrolavandulol.
Kinetic resolution of primary 2-methyl-substituted alcohols via Pseudomonas cepacia lipase-catalysed enantioselective acylation
Nordin, Ove,Nguyen, Ba-Vu,Voerde, Carin,Hedenstroem, Erik,Hoegberg, Hans-Erik
, p. 367 - 376 (2007/10/03)
The enantioselectivities of lipases from Pseudomonas cepacia (PFL, Amano PS, etc.) towards a series of primary 2-methyl-substituted alcohols using vinyl acetate as the acyl donor in transesterifications in organic solvents were studied. In terms of enantioselectivity, the best results were found for 3-aryl-2-methylpropan-1-ols with enantiomeric ratios (E-values) over 100 in most cases, whereas other 3-substituted primary 2-methylpropan-1-ols generally displayed lower enantioselectivities: 3-cycloalkyl-2-methylpropan-1-ols (E ≈ 20) and 2-methylalkan-1-ols (E ≈ 10). Moving the aryl group closer or further away from the chiral centre resulted in low enantioselectivities: 2-arylpropan-1-ols (E 10), 2-methyl-4-(2-thienyl)butan-1-ol (E = 12), 2-methyl-5-(2-thienyl)pentan-1-ol (E = 3.2) and 2-methyl-6-(2-thienyl)hexan-1-ol (E = 3.8).
