88795-86-2 Usage
Uses
Used in Fragrance and Flavor Industry:
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE is used as a fragrance ingredient for its sweet, floral odor, making it suitable for adding a pleasant scent to perfumes, soaps, and cosmetics.
Used in Food Industry:
In the food industry, 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE is used as a flavoring agent to enhance the taste and aroma of various food products.
Used in Pharmaceutical Industry:
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE has potential applications in the pharmaceutical industry, where it serves as a precursor for the synthesis of various drugs, contributing to the development of new medicinal compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 88795-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,9 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88795-86:
(7*8)+(6*8)+(5*7)+(4*9)+(3*5)+(2*8)+(1*6)=212
212 % 10 = 2
So 88795-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O2/c1-4-5-10(12)9-6-7-13-11(2,3)8-9/h9H,4-8H2,1-3H3
88795-86-2Relevant academic research and scientific papers
GENERAL RELATIONSHIPS IN THE OPENING OF THE OXIRANE RING DURING CLEAVAGE OF GLYCIDIC ACIDS
Kuroyan, R. A.,Markosyan, A. I.,Engoyan, A. P.,Vartanyan, S. A.
, p. 1709 - 1714 (2007/10/02)
By investigation of the decarboxylation of 2,3-epoxy derivatives of acids with various structures it was shown that contrary to the existing theory about the essential opening of the β (C-O) bond in the oxirane ring there are many structural types of 2,3-epoxypropionic acids, in which opening of the α (C-O) bond in the oxirane ring occurs during decarboxylation.It was also shown that these two possible reaction paths can also arise during the decarboxylation of one 2,3-epoxypropionic acid.On the basis of the obtained data a general relationship is developed for theopening of the oxirane ring during the decarboxylation of 2,3-epoxypropionic acids with any structure, and this makes it possible to predict the structure of the obtained carbonyl compound.
