139697-88-4 Usage
General Description
"[2-(2-FURYL)PHENYL]METHANOL" is a chemical compound with a molecular structure consisting of a furan ring attached to a phenyl ring, which is further linked to a methanol group. [2-(2-FURYL)PHENYL]METHANOL is used in various applications, including as a building block in organic synthesis and as a starting material for the production of pharmaceuticals and agrochemicals. It is also utilized in the fragrance and flavor industry due to its aromatic properties. Additionally, [2-(2-FURYL)PHENYL]METHANOL has potential applications in materials science for the development of new polymers and functional materials. Overall, this chemical exhibits a versatile range of uses in different industries due to its unique molecular structure and properties.
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.
