183210-33-5 Usage
Description
(5-METHYL-2-PHENYL-3-FURYL)METHANOL, also known as Anisyl alcohol, is an organic compound characterized by its floral, sweet, and slightly spicy odor. It features a furan ring, a phenyl group, and a hydroxyl group in its chemical structure, which makes it a versatile building block for synthesizing various aromatic compounds. Found in natural sources like anise oil and other essential oils, this compound holds significant value across the fragrance, flavor, and pharmaceutical industries.
Uses
Used in Perfumery:
(5-METHYL-2-PHENYL-3-FURYL)METHANOL is used as a fragrance ingredient for its floral, sweet, and slightly spicy scent, contributing to the creation of various perfumes and colognes.
Used in Flavoring Agents for Food and Beverages:
In the food and beverage industry, (5-METHYL-2-PHENYL-3-FURYL)METHANOL is used as a flavoring agent to impart its distinct aroma and taste, enhancing the sensory experience of consumable products.
Used in Pharmaceutical Production:
(5-METHYL-2-PHENYL-3-FURYL)METHANOL is used as a building block in the synthesis of pharmaceuticals, playing a crucial role in the development of various medicinal compounds.
Used in the Synthesis of Aromatic Compounds:
Due to its chemical structure, (5-METHYL-2-PHENYL-3-FURYL)METHANOL is used as a versatile intermediate in the synthesis of a wide range of aromatic compounds for different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 183210-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,2,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 183210-33:
(8*1)+(7*8)+(6*3)+(5*2)+(4*1)+(3*0)+(2*3)+(1*3)=105
105 % 10 = 5
So 183210-33-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O2/c1-9-7-11(8-13)12(14-9)10-5-3-2-4-6-10/h2-7,13H,8H2,1H3
183210-33-5Relevant articles and documents
Halomethyl derivatives of 2-phenylfurans in the Arbuzov and Michaelis-Becker reactions
Pevzner,Ignat'ev,Ionin
, p. 917 - 921 (2007/10/03)
The α-phenyl substituent in 3-(chloromethyl)furan, nonconjugated with the reaction center, does not hinder the nucleophilic attack of phosphite anion under conditions of the Michaelis-Becker reaction, while in the isomer with a conjugated phenyl substituent the halogen atom is attacked under the same conditions. Reaction of the latter with trimethyl phosphite yields the corresponding phosphonate. Phosphorylation of 5-(bromomethyl)-2-phenylfuran derivatives containing acceptor substituents in the β-position of the furan ring with trimethyl phosphite in the presence of amyl alcohol as proton donor involves no attack of the phosphite on the halogen atom and the products of the classic Arbuzov reaction are formed.
