139697-88-4 Usage
Description
[2-(2-FURYL)PHENYL]METHANOL is a chemical compound characterized by a molecular structure that features a furan ring attached to a phenyl ring, which is then connected to a methanol group. This unique arrangement endows it with a variety of properties that make it valuable in multiple industries.
Uses
Used in Organic Synthesis:
[2-(2-FURYL)PHENYL]METHANOL serves as a building block in organic synthesis, contributing to the creation of a wide range of chemical compounds. Its structural components allow it to be a key intermediate in the synthesis of more complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, [2-(2-FURYL)PHENYL]METHANOL is utilized as a starting material for the production of various drugs. Its chemical properties make it a suitable precursor for the development of new medicinal compounds.
Used in Agrochemicals:
Similarly, in the agrochemical sector, [2-(2-FURYL)PHENYL]METHANOL is employed as a starting material for the synthesis of different agrochemical products, playing a role in the development of pesticides and other agricultural chemicals.
Used in Fragrance and Flavor Industry:
Leveraging its aromatic properties, [2-(2-FURYL)PHENYL]METHANOL is used in the fragrance and flavor industry to create distinctive scents and tastes for various consumer products.
Used in Materials Science:
[2-(2-FURYL)PHENYL]METHANOL also has potential applications in materials science, particularly in the development of new polymers and functional materials. Its unique molecular structure allows it to contribute to the advancement of material technologies.
Overall, [2-(2-FURYL)PHENYL]METHANOL's versatility is evident through its applications across different industries, underscoring its importance as a chemical compound with a broad spectrum of uses.
Check Digit Verification of cas no
The CAS Registry Mumber 139697-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,6,9 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 139697-88:
(8*1)+(7*3)+(6*9)+(5*6)+(4*9)+(3*7)+(2*8)+(1*8)=194
194 % 10 = 4
So 139697-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O2/c12-8-9-4-1-2-5-10(9)11-6-3-7-13-11/h1-7,12H,8H2
139697-88-4Relevant articles and documents
Synthesis of substituted biarylmethanol via ferrocenyloxime palladacycles catalyzed suzuki reaction of chlorophenylmethanol in water
Li, Hong-Mei,Feng, Ai-Qing,Lou, Xin-Hua
, p. 2551 - 2554 (2014/09/17)
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Synthesis of biaryls by intramolecular radical transfer: Use of phosphinates
Clive, Derrick L.J.,Kang, Shunzhen
, p. 1315 - 1319 (2007/10/03)
Phosphinates 4a-13a give biaryls 4b-13b on heating with stannanes in the presence of a radical initiator. (C) 2000 Elsevier Science Ltd.
Conformational Study of Anticholinesterase Carbamates in the Furylbenzene Series by 1H and 13C NMR Spectroscopy
Platzer, N.,Ronzani, N.,Lang, C.,Lange, C.
, p. 14 - 19 (2007/10/02)
The structural analysis of carbamates derived from 2-(α-furyl)benzaldoximes and 2-(α-furyl)benzyl alcohols was carried out by 1H and 13C NMR spectroscopy.The conjugative and steric effects of alkyl substituents introduced on the benzene rings were found to modify the relative orientation of the aromatic and furan rings.The existence of a close relationship between the stereochemistry of the studied compounds and their anticholinesterase activity has been proposed.
