63791-85-5 Usage
Description
2-Ethyl-3-methyl-butanoic acidethylester, also known as ethyl 2-ethyl-3-methylbutyrate, is a chemical compound with the molecular formula C9H18O2. It is a clear, colorless liquid with a strong, pleasant, fruity, and sweet aroma. 2-Ethyl-3-methyl-butanoic acidethylester is flammable and is considered relatively safe for use in consumer products when used in accordance with regulations and guidelines.
Uses
Used in Food Industry:
2-Ethyl-3-methyl-butanoic acidethylester is used as a flavoring agent for its fruity and sweet aroma, enhancing the taste and smell of various food products.
Used in Perfume Industry:
This chemical compound is used as a fragrance ingredient in the production of perfumes, providing a pleasant and long-lasting scent.
Used in Soap and Personal Care Products:
2-Ethyl-3-methyl-butanoic acidethylester is used in the formulation of soaps and other personal care products, imparting a desirable aroma and improving the overall sensory experience of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 63791-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,9 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63791-85:
(7*6)+(6*3)+(5*7)+(4*9)+(3*1)+(2*8)+(1*5)=155
155 % 10 = 5
So 63791-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O2/c1-5-8(7(3)4)9(10)11-6-2/h7-8H,5-6H2,1-4H3
63791-85-5Relevant articles and documents
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Hudson,Hauser
, (1941)
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Deamination Reactions, 44. Decomposition of 1-Alkylcyclopropanediazonium Ions
Kirmse, Wolfgang,Rode, Jutta,Rode, Klaus
, p. 3672 - 3693 (2007/10/02)
1-Methyl- (17), 1,2-dimethyl- (41, 44), 1-propyl- (64), 1-(1-methylethyl)cyclopropanediazonium ions (80), and -1-diazonium ions (93) have been generated by alkaline cleavage of the analogous nitrosocarbamates in methanol.Cyclopropyl-allyl transformation and nucleophilic displacement were the only reactions of 17, 41, 44, and 93 while elimination and 1,2-shifts of an α-hydrogen compete increasingly with 64 and 80.The stereochemistry of ring cleavage and nucleophilic displacement has been explored, using 2-D labels in the case of 17 and 93.Cyclopropanediazonium ions (1) and 41 react stereospecifically, 17 and 44 are moderately stereoselective (ca. 85:15), and 93 is entirely unselective.The data indicate a gradual changeover from concerted to stepwise mechanisms.Appreciable stabilization of the positive charge is required to reach the SN1 extreme.
