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5554-99-4

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5554-99-4 Usage

General Description

(2-Methyl-3-furyl)methanol is a chemical compound with the formula C6H8O2. As a derivative of furan, it features a five-membered aromatic ring with four carbon atoms and one oxygen atom. The addition of a methanol group on this ring structure makes this substance an alcohol. Meanwhile, the methyl group at the second position of the ring as per the IUPAC nomenclature gives it its specific name. As for its uses, these tend to be specialized and may include roles in advanced materials, industrial chemical processes, and potentially even pharmaceuticals. As with many chemicals, correct handling and potential hazards should be well understood before using (2-Methyl-3-furyl)methanol.

Check Digit Verification of cas no

The CAS Registry Mumber 5554-99-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5554-99:
(6*5)+(5*5)+(4*5)+(3*4)+(2*9)+(1*9)=114
114 % 10 = 4
So 5554-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O2/c1-5-6(4-7)2-3-8-5/h2-3,7H,4H2,1H3

5554-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylfuran-3-yl)methanol

1.2 Other means of identification

Product number -
Other names 3-Furanmethanol,2-methyl

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:5554-99-4 SDS

5554-99-4Relevant articles and documents

Dearomatization of furans via [2,3]-Still-Wittig rearrangement

Caruana, Patrick A.,Frontier, Alison J.

, p. 10921 - 10926 (2007/10/03)

Furans and benzofurans of type 1 were dearomatized via the [2,3]-Still-Wittig rearrangement. Enol ethers 2 could be isolated or isomerized to the corresponding furans 3. The substitution pattern at the homofuranylic position had a strong influence on reaction behavior. Benzofurans rearranged with the greatest efficiency, and employment of a 3-substituted benzofuran (1; R′=CH3) allowed the creation of a quaternary carbon center.

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