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5-(Methoxymethyl)-2-methyl-3-furancarboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35340-00-2

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35340-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35340-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,4 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35340-00:
(7*3)+(6*5)+(5*3)+(4*4)+(3*0)+(2*0)+(1*0)=82
82 % 10 = 2
So 35340-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O4/c1-6-8(9(10)12-3)4-7(13-6)5-11-2/h4H,5H2,1-3H3

35340-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-(methoxymethyl)-2-methylfuran-3-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:35340-00-2 SDS

35340-00-2Downstream Products

35340-00-2Relevant academic research and scientific papers

Alcohol substitution and dehydrogenation of selenium compounds: A convenient preparation of trisubstituted furans from allyl-substituted 1,3-dicarbonyls

Tang,Huang, Xian

experimental part, p. 312 - 313 (2009/05/26)

Trisubstituted furans have been synthesised efficiently by an alcohol substitution and dehydrogenation reaction of selenocyclic enol ethers which were prepared by organoselenium-induced regioselective electrophilic intramolecular cyclisation of allyl-substituted 1,3-dicarbonyls.

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