55444-65-0 Usage
Uses
Used in the Food and Beverage Industry:
(Z)-3-Hexenal dimethyl acetal is used as a flavoring agent for its fruity and green apple-like scent, enhancing the taste and aroma of various food and beverage products.
Used in the Perfume and Personal Care Industry:
(Z)-3-Hexenal dimethyl acetal is used as a fragrance ingredient to provide a sweet, fruity aroma to perfumes and personal care products, contributing to their overall appeal and sensory experience.
Used in the Pharmaceutical Industry:
(Z)-3-Hexenal dimethyl acetal is used as an intermediate in the production of pharmaceuticals, playing a vital role in the synthesis of various medicinal compounds.
Used in the Production of Organic Compounds:
(Z)-3-Hexenal dimethyl acetal is utilized as an intermediate in the synthesis of other organic compounds, showcasing its versatility and importance in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 55444-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,4 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55444-65:
(7*5)+(6*5)+(5*4)+(4*4)+(3*4)+(2*6)+(1*5)=130
130 % 10 = 0
So 55444-65-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-4-5-6-7-8(9-2)10-3/h5-6,8H,4,7H2,1-3H3/b6-5-
55444-65-0Relevant academic research and scientific papers
Palladium-Catalyzed Triethylammonium Formate Reductions. 4. Reduction of Acetylenes to Cis Monoenes and Hydrogenolysis of Tertiary Allylic Amines
Weir, John R.,Patel, Babu A.,Heck, Richard F.
, p. 4926 - 4931 (2007/10/02)
Eight phenyl-conjugated and double bond conjugated acetylenes were reduced with triethylammonium formate and a palladium on carbon catalyst.Cis olefins were obtained in good yields in five examples. 4-Nitrodiphenylacetylene gave only 4-aminodibenzyl and (Z)-methyl non-2-en-4-ynoate gave mainly the E,Z dienoate. 1-Phenyl-3-methylbut-3-en-1-yne gave the cis diene initially, but it isomerized partially under the reaction conditions.Five tertiary allylic amines were shown to undergo hydrogenolysis with the same reducing agent and catalyst to give mixtures of two isomeric olefins in moderate to good yields.
