Welcome to LookChem.com Sign In|Join Free
  • or
6-(2,2,3-trimethylcyclopent-3-en-1-yl)hex-4-en-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65113-96-4

Post Buying Request

65113-96-4 Suppliers

Recommended suppliers

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

65113-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65113-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,1 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65113-96:
(7*6)+(6*5)+(5*1)+(4*1)+(3*3)+(2*9)+(1*6)=114
114 % 10 = 4
So 65113-96-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O/c1-5-13(15)8-6-7-12-10-9-11(2)14(12,3)4/h6,8-9,12H,5,7,10H2,1-4H3/b8-6+

65113-96-4SDS

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 (E)-6-(2,2,3-trimethylcyclopent-3-en-1-yl)hex-4-en-3-one

1.2 Other means of identification

Product number -
Other names 4-Hexen-3-one,6-(2,2,3-trimethyl-3-cyclopenten-1-yl)

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:65113-96-4 SDS

65113-96-4Downstream Products

65113-96-4Relevant academic research and scientific papers

Process for making intermediates for fragrance components from α-campholenic aldehyde

-

Page/Page column 6-7, (2008/06/13)

A two-step aldol condensation process is disclosed. α-Campholenic aldehyde (ACA) and methyl ethyl ketone (MEK) react in the presence of a base under conditions effective to produce a mixture comprising a high yield of ketol condensation products. Dehydration of the ketols in the presence of an organic sulfonic acid provides unsaturated ketones that are valuable intermediates for fragrance components for synthetic sandalwood products. Compared with the usual one-step, base-catalyzed approach, the two-step process increases the yield of all condensation products and maximizes production of the most valuable ketone isomers.

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 65113-96-4