3271-80-5 Usage
Description
Acetic acid 2-biphenylyl ester, also known as 2-Biphenylyl acetate, is a colorless to pale yellow liquid belonging to the class of aromatic esters. It has a faint, sweet, floral odor and is commonly used in various applications due to its unique properties.
Uses
Used in Fragrance and Flavoring Industry:
Acetic acid 2-biphenylyl ester is used as a fragrance and flavoring ingredient for its sweet, floral scent. It is incorporated into perfumes, colognes, and other personal care items to enhance their aroma.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, acetic acid 2-biphenylyl ester is used as a solvent in the manufacturing process. Its properties make it suitable for dissolving various compounds, aiding in the production of medications.
Used as a Chemical Intermediate:
Acetic acid 2-biphenylyl ester serves as a chemical intermediate in the production of various organic compounds. It is a key component in the synthesis of other chemicals, contributing to the creation of a wide range of products.
Used in Organic Synthesis:
This ester has potential applications in the field of organic synthesis as a reagent for creating new chemical compounds. Its reactivity and properties make it a valuable component in developing novel substances with specific functions.
Safety Precautions:
It is important to handle acetic acid 2-biphenylyl ester with care, as it may cause irritation to the skin, eyes, and respiratory tract if not used properly. Appropriate safety measures should be taken to minimize potential health risks during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3271-80-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,7 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3271-80:
(6*3)+(5*2)+(4*7)+(3*1)+(2*8)+(1*0)=75
75 % 10 = 5
So 3271-80-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O2/c1-11(15)16-14-10-6-5-9-13(14)12-7-3-2-4-8-12/h2-10H,1H3
3271-80-5Relevant articles and documents
A PdII Carbene Complex with Anthracene Side-Arms for π-Stacking on Reduced Graphene Oxide (rGO): Activity towards Undirected C–H Oxygenation of Arenes
Majeed, Maitham H.,Shayesteh, Payam,Persson, Axel R.,Wallenberg, L. Reine,Schnadt, Joachim,Wendt, Ola F.
supporting information, p. 4742 - 4746 (2018/11/27)
An N-heterocyclic carbene palladium(II) complex containing two anthracene side arms was immobilized on the surface of reduced graphene oxide (rGO) by π-stacking. The activity of the homogeneous analogue and the supported complex in undirected C–H acetoxylation reaction of arenes was studied. The results show that the catalytic efficiency in acetoxylation of benzene is improved in the immobilized materials compared to the homogeneous analogue. According to XPS analysis, the immobilized catalyst maintains the original oxidation state of PdII after the catalytic reaction.
Oxygenation of biphenyl by the reagent system Fe(MeCN)6(2+)-H2O2-Ac2O: an implication to the mechanism in mammalian metabolism.
Kotani,Midorikawa,Tanaka,Tobinaga
, p. 916 - 919 (2007/10/02)
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Metal Ion Oxidation. XI. Oxidation of Aromatic Hydroarbons and Arylacetic Acids by Heteropoly Anions Containing Ni(IV), Mn(IV) and Co(III) Ions as Central Atoms
Joensson, Lennart
, p. 761 - 768 (2007/10/02)
Heteropoly ions containing Ni(IV) and Mn(IV) as central atoms have been shown to oxidize aromatic hydrocarbons and arylacetic acids in acetic acid and acetic acid-water, yielding acetates and alcohols.The product patternof these reactions supports an outer-sphere electron transfer mechanism.Substituted arylacetic acids are decarboxylated when treated with 12-tungstocobalt(III)ate ion and 9-molybdonickel(IV)ate ion.These decarboxylation reactions are proposed to be outer-sphere electron transfer processes.
