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2-Furanmethanol, 5-methyl-a-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81779-39-7

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81779-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81779-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,7 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81779-39:
(7*8)+(6*1)+(5*7)+(4*7)+(3*9)+(2*3)+(1*9)=167
167 % 10 = 7
So 81779-39-7 is a valid CAS Registry Number.

81779-39-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-methylfuran-2-yl)(phenyl)methanol

1.2 Other means of identification

Product number -
Other names 5-methylfuran-2-yl(phenyl)methanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:81779-39-7 SDS

81779-39-7Relevant academic research and scientific papers

Cu(OTf)2 catalyzed synthesis of bis(5-methyl-2-furyl)methanes by condensation of 2-methylfuran with carbonyl compounds under solvent free conditions

Muthyala, Manoj Kumar,Rao, V. Kameswara,Kumar, Anil

, p. 1483 - 1488 (2011)

A facile and efficient one-pot three-component synthesis of bis(5-methyl-2-furyl)methanes has been achieved via the reaction of 2-methylfuran with a series of aliphatic and aromatic aldehydes and aliphatic ketones in presence of copper(II) triflate under solvent free conditions. The bis(5-methyl-2-furyl)methanes were obtained in 34%-72% yields and the catalyst was recycled up to four successive cycles without much loss in catalytic activity. Copyright

Catalytic Formal Benzylic C-H Bond Functionalization of 2,5-Dialkylfuran Derivatives with Ferrocenyl Alcohols as Alkylation Reagents

Ren, Didi,Xu, Lubin,Wang, Liang,Li, Shuai-Shuai

supporting information, p. 627 - 631 (2019/02/12)

The inert benzylic C-H bond of π-electron-rich heteroaromatic 2,5-dialkylfuran derivatives was conveniently functionalized with ferrocenyl alcohols as alkylation reagents under catalytic acidic conditions at room temperature, which features chemo- and reg

Singlet-oxygen-mediated one-pot synthesis of 3-keto-tetrahydrofurans from 2-(β-hydroxyalkyl) furans

Tofi, Maria,Koltsida, Konstantina,Vassilikogiannakis, Georgios

supporting information; experimental part, p. 313 - 316 (2009/07/04)

(Chemical Equation Presented) Photooxygenation of 2-(β-hydroxyalkyl) furans affords, in one synthetic operation and in high yields, 3-keto-tetrhydrofuran motifs via intramolecular Michael-type addition to the 1,4-enedione intermediate.

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