122-44-1 Usage
Uses
Used in Fragrance Industry:
3-phenylpropyl phenylacetate is used as a fragrance ingredient for its sweet, floral scent, contributing to the overall aroma profile of perfumes and colognes. Its pleasant aroma is sought after for enhancing the fragrance of these products, providing a unique and appealing scent experience.
Used in Flavor Industry:
In the flavor industry, 3-phenylpropyl phenylacetate is utilized as a flavoring agent in a variety of food and beverage products. Its sweet, floral scent translates into a desirable taste profile, enriching the flavor of these products and offering consumers a more enjoyable sensory experience.
Used in Consumer Goods Production:
3-phenylpropyl phenylacetate is a key component in the production of scented and flavored consumer goods. Its versatility allows it to be incorporated into a wide range of products, from personal care items to household products, enhancing their appeal through improved fragrance and taste.
Check Digit Verification of cas no
The CAS Registry Mumber 122-44-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122-44:
(5*1)+(4*2)+(3*2)+(2*4)+(1*4)=31
31 % 10 = 1
So 122-44-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O2/c18-17(14-16-10-5-2-6-11-16)19-13-7-12-15-8-3-1-4-9-15/h1-6,8-11H,7,12-14H2
122-44-1Relevant academic research and scientific papers
Carbene radicals in cobalt(II)-porphyrin-catalysed carbene carbonylation reactions; A catalytic approach to ketenes
Paul, Nanda D.,Chirila, Andrei,Lu, Hongjian,Zhang, X. Peter,Debruin, Bas
supporting information, p. 12953 - 12958 (2013/10/01)
One-pot radicals: Cobalt(III)-carbene radicals, generated by metallo-radical activation of diazo compounds and N-tosylhydrazone sodium salts with cobalt(II) complexes of porphyrins, readily undergo radical addition to carbon monoxide, allowing the catalytic production of ketenes. These ketenes subsequently react with various amines, alcohols and imines in one-pot tandem transformations to produce differently substituted amides, esters and β-lactams in good isolated yields. Copyright
A facile and efficient one-step conversion of alcohol triphenylmethyl ethers to the corresponding acetates
Kobayashi, Kumiko,Watahiki, Tsutomu,Oriyama, Takeshi
, p. 484 - 486 (2007/10/03)
Alcohol triphenylmethyl (trityl) ethers were readily and efficiently transformed into the corresponding acetates by reaction with acetyl bromide. Triphenylmethyl ethers can also be transformed into the corresponding substituted acetates in high yields by the use of various substituted acetyl chlorides combined with sodium iodide.
