Welcome to LookChem.com Sign In|Join Free
  • or
ω-Hydroxyundec-9-enoic acid, also known as 10-hydroxy-10-undecenoic acid, is a naturally occurring organic compound characterized by a carboxylic acid functional group and a hydroxyl group. It features an 11-carbon chain with a double bond between the 9th and 10th carbon atoms, and a hydroxyl group attached to the terminal carbon. This molecule is found in various plants and is known for its potential applications in the pharmaceutical and chemical industries. It is often associated with anti-inflammatory and antimicrobial properties, making it a subject of interest for researchers exploring its therapeutic potential.

79868-94-3

Post Buying Request

79868-94-3 Suppliers

Recommended suppliers

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

79868-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79868-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,6 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79868-94:
(7*7)+(6*9)+(5*8)+(4*6)+(3*8)+(2*9)+(1*4)=213
213 % 10 = 3
So 79868-94-3 is a valid CAS Registry Number.

79868-94-3Downstream Products

79868-94-3Relevant academic research and scientific papers

The cross-metathesis of methyl oleate with c/s-2-butene-1,4-diyl diacetate and the influence of protecting groups

Behr, Arno,Gomes, Jessica Perez

, p. 1 - 8 (2011)

Background: α,ω-Difunctional substrates are useful intermediates for polymer synthesis. An attractive, sustainable and selective (but as yet unused) method in the chemical industry is the oleochemical cross-metathesis with preferably symmetric functionalised substrates. The current study explores the cross-metathesis of methyl oleate (1) with cis-2-butene-1,4-diyl diacetate (2) starting from renewable resources and quite inexpensive base chemicals. Results: This cross-metathesis reaction was carried out with several phosphine and N-heterocyclic carbene ruthenium catalysts. The reaction conditions were optimised for high conversions in combination with high cross-metathesis selectivity. The influence of protecting groups present in the substrates on the necessary catalyst loading was also investigated. Conclusions: The value-added methyl 11-acetoxyundec-9-enoate (3) and undec-2-enyl acetate (4) are accessed with nearly quantitative oleochemical conversions and high cross-metathesis selectivity under mild reaction conditions. These two cross-metathesis products can be potentially used as functional monomers for diverse sustainable polymers.

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 79868-94-3