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696-71-9

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696-71-9 Usage

Description

Cyclooctanol is a clear, colorless liquid that serves as a crucial starting material in the chemical industry, particularly for the preparation of cyclooctanone using a chromic acid reagent.

Uses

Used in Chemical Synthesis:
Cyclooctanol is used as a key starting material for the synthesis of cyclooctanone, which is an important intermediate in the production of various chemicals and pharmaceuticals.
Used in Pharmaceutical Industry:
Cyclooctanol is utilized as a precursor in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Industrial Chemical Production:
Cyclooctanol plays a significant role in the production of industrial chemicals, as it can be converted into cyclooctanone, which is further used to manufacture other valuable compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 696-71-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 696-71:
(5*6)+(4*9)+(3*6)+(2*7)+(1*1)=99
99 % 10 = 9
So 696-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c9-8-6-4-2-1-3-5-7-8/h8-9H,1-7H2

696-71-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name CYCLOOCTANOL

1.2 Other means of identification

Product number -
Other names InChI=1/C8H16O/c9-8-6-4-2-1-3-5-7-8/h8-9H,1-7H2

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:696-71-9 SDS

696-71-9Relevant articles and documents

Catalytic oxyfunctionalization of saturated hydrocarbons by non-heme oxo-bridged diiron(III) complexes: role of acetic acid on oxidation reaction

Agarwalla, Uday Sankar

, p. 583 - 588 (2020)

Oxo-bridged diiron(III) complexes [Fe2O(L1)2(H2O)2](ClO4)4 (1) and [Fe2O(L2)2(H2O)2](ClO4)4 (2), where L1 and L2 are tetradentate N-donor N,N′-bis(2-pyridylmethyl)-1,2-cyclohexanediamine and N,N′-bis(2-pyridylmethyl)ethane-1,2-diamine respectively, have been isolated as synthetic models of non-heme iron oxygenases and characterized by physicochemical and spectroscopic methods. Both the complexes have been studied as catalysts for the oxyfunctionalization of saturated hydrocarbons using green hydrogen peroxide (H2O2) as oxidant under mild conditions. The selectivity (A/K) and regioselectivity (3°/2°) in oxidative C–H functionalization of alkanes suggests the involvement of metal-based intermediate in the oxygenation reaction. The catalytic efficiency is found to be strongly dependent on the presence of acetic acid. Remarkable increase in conversion and selectivity favoring the formation of alcohols in the oxidation of cyclohexane and cyclooctane and exclusive hydroxylation of adamantane with drastic enhancement of regioselectivity has been achieved by the addition of acetic acid in the presence of H2O2.

Pyridazine N-Oxides as Photoactivatable Surrogates for Reactive Oxygen Species

Basistyi, Vitalii S.,Frederich, James H.

supporting information, p. 1907 - 1912 (2022/03/27)

A method for the photoinduced evolution of atomic oxygen from pyridazine N-oxides was developed. This underexplored oxygen allotrope mediates arene C-H oxidation within complex, polyfunctional molecules. A water-soluble pyridazine N-oxide was also developed and shown to promote photoinduced DNA cleavage in aqueous solution. Taken together, these studies highlight the utility of pyridazine N-oxides as photoactivatable O(3P) precursors for applications in organic synthesis and chemical biology.

Pincerlike molybdenum complex and preparation method thereof, catalytic composition and application thereof, and alcohol preparation method

-

Paragraph 0134-0140, (2021/08/11)

The invention discloses a clamp-type molybdenum complex, a preparation method, a corresponding catalyst composition and application. The method comprises the steps: obtaining 9 molybdenum complexes with different structures through coordination reaction of 2-(substituent ethyl)-(5, 6, 7, 8-tetrahydroquinolyl) amine and a corresponding carbonyl molybdenum metal precursor; and catalyzing a ketone compound transfer hydrogenation reaction through a molybdenum complex to generate 40 alcohol compounds. The preparation method of the molybdenum complex is simple, high in yield and good in stability. For a transfer hydrogenation reaction of ketone, the molybdenum-based catalytic system has high catalytic activity and small molybdenum loading capacity, is used for production of aromatic and aliphatic alcohols, and has the advantages of simple method, small environmental pollution and high yield.

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