121361-47-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 13 carbon (C) atoms, 16 hydrogen (H) atoms, and 4 oxygen (O) atoms.
Explanation
The compound is versatile and finds applications in various industries due to its unique properties.
Explanation
The compound is known for its pleasant and attractive scent, which makes it suitable for use in perfumes, soaps, and cosmetics.
Explanation
The compound is used in these industries due to its properties as a solvent, fragrance ingredient, plasticizer, and flavoring agent.
Explanation
When used responsibly and within the recommended guidelines, the compound is deemed safe for use in various consumer products. However, it is essential to follow the regulations to ensure safety and avoid potential health risks.
Common Uses
Solvent, fragrance ingredient, plasticizer, and flavoring agent
Odor
Fruity, floral, and sweet
Industries
Perfumes, soaps, cosmetics, and food industry
Safety
Considered safe for use in consumer products when used in accordance with regulations and guidelines
Check Digit Verification of cas no
The CAS Registry Mumber 121361-47-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,3,6 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121361-47:
(8*1)+(7*2)+(6*1)+(5*3)+(4*6)+(3*1)+(2*4)+(1*7)=85
85 % 10 = 5
So 121361-47-5 is a valid CAS Registry Number.
121361-47-5Relevant articles and documents
Efficient and regioselective ring-opening of epoxides with carboxylic acid catalyzed by graphite oxide
Mirza-Aghayan, Maryam,Tavana, Mahdieh Molaee,Niazi, Elaheh Golam Alipour,Boukherroub, Rabah
, p. 532 - 538 (2020/07/17)
An efficient, simple and regioselective ring-opening reaction of epoxides with various carboxylic acids under metal-free conditions is reported. The ring-opening of epoxides takes place in the presence of graphite oxide as an efficient and available catalyst to produce the corresponding 2-hydroxy monoester and 1,2-diester derivatives in good yields. Regioselective attack of the nucleo-phile, short reaction times, metal-free conditions and reusability of catalyst are among the advantages of the present protocol.
Enzymatic Resolution of 1,2-Diols: Comparison between Hydrolysis and Transesterification Reactions
Bosetti, Aldo,Bianchi, Daniele,Cesti, Pietro,Golini, Paolo,Spezia, Sandro
, p. 2395 - 2398 (2007/10/02)
A new practical procedure for the enzymatic resolution of 1,2-diols 1a-e has been developed by lipase-catalysed regio- and enantio-selective esterification using anhydrides as acylating agents in organic solvents.
OXIDATION OF ISOXAZOLINES BY PERACIDS - A USEFUL ROUTE TO β-HYDROXY KETONES AND ACYLATED DIOLS
Park, Pyeong-uk,Kozikowski, Alan P.
, p. 6703 - 6706 (2007/10/02)
A method for bringing about the ring cleavage of isoxazolines by the use of peracids is described.
