88795-87-3 Usage
Description
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is a chemical compound characterized by its molecular formula C12H22O. It is a ketone with a distinctive carbonyl group bonded to two carbon atoms, and is recognized for its fruity, floral scent.
Used in Fragrance Industry:
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is used as a fragrance additive for its appealing fruity and floral odor, enhancing the scent profiles of various perfumes and personal care products.
Used in Flavor Industry:
In the flavor industry, 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is utilized as a flavoring agent, imparting its unique taste to food products, thereby enriching their sensory experience.
Used in Pharmaceutical Development:
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is also being explored for its potential pharmaceutical applications, particularly in the development of new drugs, capitalizing on its chemical properties for therapeutic benefits.
Safety Note:
As with many chemicals, 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE should be handled with care and in accordance with established safety guidelines to ensure the well-being of users and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 88795-87-3 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 88795-87:
(7*8)+(6*8)+(5*7)+(4*9)+(3*5)+(2*8)+(1*7)=213
213 % 10 = 3
So 88795-87-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-4-5-6-11(13)10-7-8-14-12(2,3)9-10/h10H,4-9H2,1-3H3
88795-87-3Relevant articles and documents
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.