3271-80-5

Basic information

• Product Name: Acetic acid 2-biphenylyl ester
• Synonyms: 1,1'-Biphenyl-2-ol acetate;2-Acetoxy-1,1'-biphenyl;2-Acetoxybiphenyl;2-Phenylphenyl acetate;Acetic acid 2-biphenylyl ester;[1,1'-Biphenyl]-2-yl acetate
• CAS NO: 3271-80-5
• Molecular Formula: C₁₄H₁₂O₂
• Molecular Weight: 212.25
• Mol File: 3271-80-5.mol
• Article Data: 7

Chemical Properties

• Melting Point: 63-63.5 °C
• Boiling Point: 341.6°Cat760mmHg
• Flash Point: 118°C
• Appearance: /
• Density: 1.103g/cm³
• Vapor Pressure: 7.98E-05mmHg at 25°C
• Refractive Index: 1.559
• CAS DataBase Reference: Acetic acid 2-biphenylyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid 2-biphenylyl ester(3271-80-5)
• EPA Substance Registry System: Acetic acid 2-biphenylyl ester(3271-80-5)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 3271-80-5(Hazardous Substances Data)

Usage

General Description

Acetic acid 2-biphenylyl ester, also known as 2-Biphenylyl acetate, is a chemical compound that belongs to the class of aromatic esters. It is a colorless to pale yellow liquid with a faint, sweet, floral odor. This chemical is commonly used as a fragrance and flavoring ingredient in various products, such as perfumes, colognes, and other personal care items. It is also used as a solvent in the manufacturing of pharmaceuticals and as a chemical intermediate in the production of various organic compounds. Additionally, acetic acid 2-biphenylyl ester has potential applications in the field of organic synthesis as a reagent for creating new chemical compounds. However, it is important to handle this chemical with care, as it may cause irritation to the skin, eyes, and respiratory tract if not used properly.

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

Upstream product

• 92-52-4 biphenyl 
• 33035-41-5 2-(diacetoxyiodo)mesitylene 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 64-19-7 acetic acid 
• 108-24-7 acetic anhydride 
• 52602-01-4 tert-butyl acetylperoxysalicylate 
• 127-09-3 sodium acetate 

Downstream Products

• 136131-40-3 5-phenyl-1,4-dihydro-1,4-epoxynaphthalene 
• 21424-82-8 1-(2-hydroxy-[1,1'-biphenyl]-3-yl)ethanone 
• 57018-28-7 acetic acid-(5-bromo-biphenyl-2-yl ester) 
• 65594-67-4 biphenyl-2,2′-diyldiacetate 
• 58244-28-3 2,5-diacetoxybiphenyl 
• 111625-10-6 2,4'-diacetoxybiphenyl 
• 90-43-7 2-Phenylphenol 
• 500308-27-0 acetic acid-(3,5-dibromo-biphenyl-2-yl ester) 
• 34743-37-8 2-Phenyl-4-acetylphenoxy-2,6-dimethylphenylimino-methansulfensaeure 
• 34743-60-7 (2,6-Dimethyl-phenyl)-thiocarbamic acid O-(5-acetyl-biphenyl-2-yl) ester 
• 34743-67-4 C₁₅H₁₁ClO₂S 
• 55815-20-8 3,5-dibromo-2-hydroxybiphenyl 
• 92495-65-3 5-ethyl-biphenyl-2-ol 
• 16434-97-2 5-bromo-[1,1′-biphenyl]-2-ol 

Relevant 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

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.

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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

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.