143291-83-2 Usage
General Description
3-[3-(benzyloxy)phenyl]-2-methylpropan-1-ol is a chemical compound with the molecular formula C20H22O2. It is an organic compound that belongs to the class of alcohols. 3-[3-(benzyloxy)phenyl]-2-methylpropan-1-ol consists of a benzene ring with an attached benzyloxy group and a phenyl group, as well as a 2-methylpropan-1-ol group. It can be used in various chemical reactions and processes due to its unique structure and properties. The compound may have potential applications in the pharmaceutical industry, as well as in the synthesis of other organic compounds. Additionally, it may also have industrial uses, such as in the production of fragrances or flavorings. Overall, the chemical 3-[3-(benzyloxy)phenyl]-2-methylpropan-1-ol has potential significance in various fields due to its molecular structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 143291-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,9 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143291-83:
(8*1)+(7*4)+(6*3)+(5*2)+(4*9)+(3*1)+(2*8)+(1*3)=122
122 % 10 = 2
So 143291-83-2 is a valid CAS Registry Number.
143291-83-2Relevant articles and documents
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).
