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1-N-PROPYLCYCLOHEXANOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5445-24-9

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5445-24-9 Usage

Uses

Intermediates of Liquid Crystals

Check Digit Verification of cas no

The CAS Registry Mumber 5445-24-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5445-24:
(6*5)+(5*4)+(4*4)+(3*5)+(2*2)+(1*4)=89
89 % 10 = 9
So 5445-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O/c1-2-6-9(10)7-4-3-5-8-9/h10H,2-8H2,1H3

5445-24-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (B20946)  1-n-Propylcyclohexanol, 98%   

  • 5445-24-9

  • 5g

  • 333.0CNY

  • Detail

  • Alfa Aesar

  • (B20946)  1-n-Propylcyclohexanol, 98%   

  • 5445-24-9

  • 25g

  • 1329.0CNY

  • Detail

5445-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-propylcyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Hydroxy-1-propyl-cyclohexan

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:5445-24-9 SDS

5445-24-9Relevant academic research and scientific papers

Tandem cross-metathesis/hydrogenation/cyclization reactions by using compatible catalysts

Cossy, Janine,Bargiggia, Frederic,BouzBouz, Samir

, p. 459 - 462 (2007/10/03)

(Matrix presented) A one-pot tandem cross-metathesis/hydrogenation/cyclization procedure was achieved at room temperature, under 1 atm of hydrogen, in the presence of a ruthenium catalyst and PtO2 showing the compatibility of the two catalysts. This tandem reaction allows the synthesis of substituted lactones and lactols from acrylic acid and acrolein, respectively, in the presence of unsaturated alcohols.

THE PREPARATION OF LITHIUM ORGANOCUPRATES FROM VARIOUS Cu(I) SALTS

Bertz, Steven H.,Gibson, Charles P.,Dabbagh, Gary

, p. 4251 - 4254 (2007/10/02)

Various Cu(I) salts have been tested as precursors for organocuprates in side-by-side comparisons under controlled conditions.CuCN and CuBr*SMe2 appear to be superior to CuI, CuBr, and CuCl.CuSCN and CuOTf are also good precursors in some circumstances.

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