87247-19-6 Usage
Description
(2S)-6-Methylheptan-2-ol, also known as 6-Methylheptan-2-ol, is a colorless liquid compound with a chemical formula of C8H18O. It is classified as a secondary alcohol and is widely recognized for its pleasant, fruity aroma.
Uses
Used in Fragrance and Flavor Industry:
(2S)-6-Methylheptan-2-ol is used as a fragrance and flavoring agent for its pleasant, fruity aroma, enhancing the sensory experience of various consumer products.
Used in Chemical Production:
(2S)-6-Methylheptan-2-ol is used as a solvent or a chemical intermediate, playing a crucial role in the synthesis of other chemicals, thereby contributing to the chemical industry's diverse applications.
Used in Agricultural Applications:
(2S)-6-Methylheptan-2-ol is used as an antimicrobial and insecticidal agent, helping to protect crops and improve agricultural yields by controlling pests and diseases.
Used in Pharmaceutical Applications:
(2S)-6-Methylheptan-2-ol is utilized for its antimicrobial properties, potentially contributing to the development of new treatments and therapies in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 87247-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,4 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87247-19:
(7*8)+(6*7)+(5*2)+(4*4)+(3*7)+(2*1)+(1*9)=156
156 % 10 = 6
So 87247-19-6 is a valid CAS Registry Number.
87247-19-6Relevant articles and documents
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Doering,Young
, (1952)
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Chiral surfactant-type catalyst for asymmetric reduction of aliphatic ketones in water
Li, Jiahong,Tang, Yuanfu,Wang, Qiwei,Li, Xuefeng,Cun, Linfeng,Zhang, Xiaomei,Zhu, Jin,Li, Liangchun,Deng, Jingen
supporting information, p. 18522 - 18525 (2013/01/15)
A novel chiral surfactant-type catalyst is developed. Micelles formed in water by association of the catalysts themselves, and this was confirmed by TEM analyses. Asymmetric transfer hydrogenation of aliphatic ketones catalyzed by the chiral metallomicellar catalyst gave good to excellent conversions and remarkable stereoselectivities (up to 95% ee). Synergistic effects between the metal-catalyzed center and the hydrophobic microenvironment of the core in the metallomicelle led to high enantioselectivities.
Asymmetric reduction of ketones by Geotrichum candidum in the presence of Amberlite Xad, A solid organic solvent
Nakamura, Kaoru,Fujii, Mikio,Ida, Yoshiteru
, p. 3205 - 3211 (2007/10/03)
Asymmetric reduction of ketones by Geotrichum candidum in the presence of Amberlite XAD, a solid organic solvent, was described. A hydrophobic polymer, XAD, was used as material to control the stereochemical course of microbial reductions. Aliphatic and aromatic ketones were reduced to the corresponding (S)-alcohols in excellent enantiomeric excess (ee) in the presence of XRD while low enantioselectivities were observed in the absence of the polymer.
