Welcome to LookChem.com Sign In|Join Free
  • or
cyclohexylmethyl cyclohexylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86328-74-7

Post Buying Request

86328-74-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

86328-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86328-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,2 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86328-74:
(7*8)+(6*6)+(5*3)+(4*2)+(3*8)+(2*7)+(1*4)=157
157 % 10 = 7
So 86328-74-7 is a valid CAS Registry Number.

86328-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexylmethyl 2-cyclohexylacetate

1.2 Other means of identification

Product number -
Other names cyclohexylmethyl cyclohexylacetate

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:86328-74-7 SDS

86328-74-7Upstream product

86328-74-7Downstream Products

86328-74-7Relevant academic research and scientific papers

Well-defined iron catalysts for the acceptorless reversible dehydrogenation-hydrogenation of alcohols and ketones

Chakraborty, Sumit,Lagaditis, Paraskevi O.,F?rster, Moritz,Bielinski, Elizabeth A.,Hazari, Nilay,Holthausen, Max C.,Jones, William D.,Schneider, Sven

, p. 3994 - 4003 (2014)

Acceptorless dehydrogenation of alcohols, an important organic transformation, was accomplished with well-defined and inexpensive iron-based catalysts supported by a cooperating PNP pincer ligand. Benzylic and aliphatic secondary alcohols were dehydrogenated to the corresponding ketones in good isolated yields upon release of dihydrogen. Primary alcohols were dehydrogenated to esters and lactones, respectively. Mixed primary/secondary diols were oxidized at the secondary alcohol moiety with good chemoselectivity. The mechanism of the reaction was investigated using both experiment and DFT calculations, and the crucial role of metal-ligand cooperativity in the reaction was elucidated. The iron complexes are also excellent catalysts for the hydrogenation of challenging ketone substrates at ambient temperature under mild H2 pressure, the reverse of secondary alcohol dehydrogenation.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 86328-74-7