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Detail of "14898-86-3"

  • CAS Number:
  • 14898-86-3
  • Name:
  • Benzenemethanol, α-(1-methylethyl)-, (αR)-

  • Molecular Structure:
  • Formula:
  • C10H14O
  • Molecular Weight:
  • 150.22
  • Synonyms:
  • Benzenemethanol, a-(1-methylethyl)-,(R)-;Benzyl alcohol, a-isopropyl-, (R)-(+)- (8CI);(+)-(aR)-a-(1-Methylethyl)benzenemethanol;(+)-a-Isopropylbenzylalcohol;(1R)-2-Methyl-1-phenylpropan-1-ol;(R)-(+)-2-Methyl-1-phenyl-1-propanol;(R)-1-Phenyl-2-methyl-1-propanol;(R)-1-Phenyl-2-methylpropanol;(R)-2-Methyl-1-phenyl-1-propanol;(R)-a-(1-Methylethyl)benzenemethanol;(R)-a-Isopropylbenzylalcohol;
  • Density:
  • 0.976 g/cm3
  • Boiling Point:
  • 219.8 °C at 760 mmHg
  • Flash Point:
  • 86.7 °C
  • Risk Codes:
  • 22
  • Safety:
  • 36/37 Details

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CAS No.14898-86-3 Benzenemethanol, α-(1-methylethyl)-, (αR)-

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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CAS No.14898-86-3 Benzenemethanol, α-(1-methylethyl)-, (αR)-

Supplier:Waterstone Technology, LLC [ United States]

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CAS No.14898-86-3 Benzenemethanol, α-(1-methylethyl)-, (αR)-

Supplier:CHEMSWORTH [ India]

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CAS No.14898-86-3 Benzenemethanol, α-(1-methylethyl)-, (αR)-

Supplier:Carbone scientific [ United Kingdom]

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Address:London, UK

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Reference

Side chain oxidation of aromatic compounds by fungi
7. A rationale for sulfoxidation, benzylic hydroxylation, and olefin oxidation by Mortierella isabellina. Holland, Herbert L.; Allen, Lisa J.; Chernishenko, Michael J.; Diez, Manuel; Kohl, Andreas; Ozog, John; Gu, Jian-Xin (Dep. Chem.There are some reagents like 14898-86-3 is used in this study., Brock Univ., St. Catharines, ON, Can.). Journal of Molecular Catalysis B: Enzymatic, 3(6), 311-324 (English) 1997 Elsevier. CODEN: JMCEF8. ISSN: 1381-1177. DOCUMENT TYPE: Journal CA Section: 10 (Microbial, Algal, and Fungal Biochemistry) Section cross-reference(s): 16 The fungus M. isabellina ATCC 42613 catalyzes the biotransformation of substituted-aryl Me sulfides to give sulfoxides of predominantly (R) configuration, of aryl-substituted alkenes to give chiral vicinal diols, and of various phenylalkanes and phenylcycloalkanes to give (R)-configuration benzylic alcs. The nature of the products from all these processes may be accounted for by a single model based on restrictive space descriptors that can be used to rationalize these reactions, and which is proposed as a predictor of the outcome of the M. isabellina-catalyzed oxidns. of similar substrates. .
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