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Source: The Open Library

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1Étude de la décomposition catalytique du dihydroxyperoxyde de cyclohexyle et de l'hydroxy-hydroperoxyde de cyclohexyle

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“Étude de la décomposition catalytique du dihydroxyperoxyde de cyclohexyle et de l'hydroxy-hydroperoxyde de cyclohexyle” Metadata:

  • Title: ➤  Étude de la décomposition catalytique du dihydroxyperoxyde de cyclohexyle et de l'hydroxy-hydroperoxyde de cyclohexyle
  • Author:
  • Language: fre
  • Number of Pages: Median: 70
  • Publisher: Institut français du pétrole
  • Publish Date:
  • Publish Location: Rueil-Malmaison

“Étude de la décomposition catalytique du dihydroxyperoxyde de cyclohexyle et de l'hydroxy-hydroperoxyde de cyclohexyle” Subjects and Themes:

Edition Identifiers:

  • The Open Library ID: OL57215002M
  • Online Computer Library Center (OCLC) ID: 3826258
  • Library of Congress Control Number (LCCN): 74327052

Access and General Info:

  • First Year Published: 1971
  • Is Full Text Available: No
  • Is The Book Public: No
  • Access Status: No_ebook

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Cyclohexanol

Cyclohexanol is the organic compound with the formula HOCH(CH2)5. The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl

4-Phenyl-4-(1-piperidinyl)cyclohexanol

4-Phenyl-4-(1-piperidinyl)cyclohexanol, also known as PPC, is an organic chemical which is a metabolite of phencyclidine (PCP). It can be detected in the

Isobornyl cyclohexanol

Isobornyl cyclohexanol (IBCH, Sandenol) is an organic compound used primarily as a fragrance because of its aroma which is similar to sandalwood oil. Its

Cyclohexanol dehydrogenase

In enzymology, a cyclohexanol dehydrogenase (EC 1.1.1.245) is an enzyme that catalyzes the chemical reaction cyclohexanol + NAD+ ⇌ {\displaystyle \rightleftharpoons

Cyclohexanone

hydrogen to cyclohexanol, which he wasn't able to isolate, and then oxidized by electrolytic oxygen. Cyclohexanone can be prepared from cyclohexanol by oxidation

Trans-2-Phenyl-1-cyclohexanol

trans-2-Phenyl-1-cyclohexanol is an organic compound. The two enantiomers of this compound are used in organic chemistry as chiral auxiliaries. The enantioselective

Cyclohexane

autoxidation to give a mixture of cyclohexanone and cyclohexanol. The cyclohexanone–cyclohexanol mixture, called "KA oil", is a raw material for adipic

Cyclohexene

than benzene. In the laboratory, it can be prepared by dehydration of cyclohexanol. C6H11OH → C6H10 + H2O Benzene is converted to cyclohexylbenzene by acid-catalyzed

Cyclohexyl chloride

It is a colorless liquid. Cyclohexyl chloride can be prepared from cyclohexanol by treatment with hydrogen chloride. Henry Gilman and W. E. Catlin (1926)

Chiral auxiliary

compound is difficult to prepare and as an alternative trans-2-phenyl-1-cyclohexanol was introduced by J. K. Whitesell in 1985. Chiral auxiliaries are incorporated