Welcome to LookChem.com Sign In|Join Free
  • or
Trimethyl-4,6,6-heptene-4-one-2 is a complex organic compound with the molecular formula C10H18O. It is a colorless liquid with a strong, pungent odor. This chemical is primarily used as a fragrance ingredient in various consumer products, such as perfumes, cosmetics, and personal care items. It is known for its ability to provide a fresh, citrusy scent, which is often reminiscent of lemon or orange. The compound is synthesized through a series of chemical reactions and is carefully controlled for purity and quality to ensure it meets the stringent safety standards required for use in personal care products. It is important to note that while it is used in fragrances, the specific safety and usage guidelines should be followed, as the compound's properties and potential effects can vary based on concentration and application.

81787-11-3

Post Buying Request

81787-11-3 Suppliers

Recommended suppliers

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

81787-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81787-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,8 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81787-11:
(7*8)+(6*1)+(5*7)+(4*8)+(3*7)+(2*1)+(1*1)=153
153 % 10 = 3
So 81787-11-3 is a valid CAS Registry Number.

81787-11-3Downstream Products

81787-11-3Relevant academic research and scientific papers

FORMATION DE CETONES ETHYLENIQUES PAR ACTION D'ACIDE ACETYLSULFOACETIQUE SUR DES ALCENES

Loiseau, Andre-Michel,Luft, Robert,Zunino, Serge

, p. 144 - 152 (2007/10/02)

Monoalkyl- and 1,2-dialkylethylenes have a similar behaviour under the action of acetylsulfoacetic acid : the reaction does not necessarily stop after the formation of α- or β-enones, the yield of which is highly influenced by reaction time; thus, 1-acetoxy-1,3-dienes are identified in the case of α-enones.A different behaviour is shown by 1,1-dialkyl and trialkylethylenes, which can constitute an interesting source of highly branched enones.With this second group of alkenes, isomerisation of the alkene is sometimes observed prior to acetylation.Lastly, some alkenes undergo acetoxylation at the same time as acetylation.

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 81787-11-3