90036-85-4 Usage
Uses
Used in Perfumery Industry:
(2Z)-3-ethoxybut-2-en-1-ol is utilized as a key ingredient in the production of perfumes, where its sweet, floral scent adds depth and complexity to fragrances.
Used in Flavorings Industry:
In the flavorings industry, (2Z)-3-ethoxybut-2-en-1-ol serves as a component to enhance the taste and aroma of various food and beverage products, capitalizing on its pleasant odor and flavor profile.
Used in Fragrance Products:
(2Z)-3-ethoxybut-2-en-1-ol is also employed in the creation of other fragrance products, such as candles, air fresheners, and personal care items, to provide a pleasant and appealing scent.
Used as a Precursor in Organic Synthesis:
(2Z)-3-ethoxybut-2-en-1-ol is used as a precursor in the synthesis of other organic compounds, highlighting its importance in the realm of organic chemistry and the production of various chemical products.
Used in Pharmaceutical Industry:
Within the pharmaceutical sector, (2Z)-3-ethoxybut-2-en-1-ol finds applications due to its chemical properties, potentially contributing to the development of new drugs and medicinal compounds.
Used in Biotechnology:
In the field of biotechnology, (2Z)-3-ethoxybut-2-en-1-ol may have specific uses, possibly related to its ability to participate in biochemical processes or as a component in biotechnological products.
Check Digit Verification of cas no
The CAS Registry Mumber 90036-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,3 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90036-85:
(7*9)+(6*0)+(5*0)+(4*3)+(3*6)+(2*8)+(1*5)=114
114 % 10 = 4
So 90036-85-4 is a valid CAS Registry Number.
90036-85-4Relevant academic research and scientific papers
Iridium-catalyzed asymmetric hydrogenation of vinyl ethers
Zhu, Ye,Burgess, Kevin
supporting information; experimental part, p. 979 - 983 (2009/05/30)
A carbene-oxazoline catalyst 1 proved to be an effective catalyst for reduction of an enol ether that the literature suggested could not be hydrogenated effectively by P,N-Ir catalysts. Thus, a series of ester and alcohol substrates were hydrogenated using catalyst 1. Good to excellent enantioselectivities and high conversions were obtained.
Latent Inhibitors. Part 2. Allylic Inhibitors of Alcohol Dehydrogenase
MacInnes, Iain,Schorstein, David E.,Suckling, Colin J.,Wrigglesworth, Roger
, p. 1103 - 1108 (2007/10/02)
The syntheses of a number of 3-substituted prop-2-en-1-ols and -1-als, required for studying the latent inhibition of horse liver alcohol dehydrogenase (E.C. 1.1.1.1), are described.Substituent were chosen to cover a range of alkoxide, phenolate, thiolate
