88795-87-3 Usage
General Description
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is a chemical compound with the molecular formula C12H22O. It is known for its fruity, floral odor and is commonly used in the fragrance and flavor industry. 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is a ketone, which means it contains a carbonyl group bonded to two carbon atoms. It is often used as a flavoring agent in food products and as a fragrance additive in perfumes and personal care products. Additionally, it has been studied for its potential pharmaceutical applications, particularly in the development of new drugs. However, like many chemicals, it should be handled with care and in accordance with safety guidelines.
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.
