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154222-96-5

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154222-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154222-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,2,2 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 154222-96:
(8*1)+(7*5)+(6*4)+(5*2)+(4*2)+(3*2)+(2*9)+(1*6)=115
115 % 10 = 5
So 154222-96-5 is a valid CAS Registry Number.

154222-96-5SDS

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 3-Furancarboxylicacid,4-methyl-,ethylester(9CI)

1.2 Other means of identification

Product number -
Other names MC 9761

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:154222-96-5 SDS

154222-96-5Upstream product

154222-96-5Downstream Products

154222-96-5Relevant articles and documents

Synthesis of five-membered heterocycles by indirect electrochemical approach in Green media

Dures,Lombard,Pereira,Esteves,Medeiros

, p. G1 - G7 (2015/04/21)

Radical cyclization continues to be a central methodology for the preparation of natural products containing heterocyclic rings. Hence, some electrochemical results obtained by cyclic voltammetry and controlled-potential electrolysis in the study of electroreductive intramolecular cyclization of ethyl (2S, 3R)-2-bromo-3-propargyloxy-3-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyloxy) propanoate (1a), 2-bromo-3-allyloxy-3-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyloxy)propanoate (1b), 2-bromo-[1-(prop-2-yn-1-yloxy)propyl]benzene (1c) and [1-bromo-2-methoxy-2-(prop-2′-yn-1-yloxy)ethyl]benzene (1d) promoted by (1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane)nickel(I), [Ni(tmc)]+, electrogenerated at glassy carbon cathodes in ethanol and ethanol:water mixtures containing tetraalkylammonium salts, are presented. During controlled-potential electrolyses of solutions containing [Ni(tmc)]2+ and bromoalkoxylated compounds (1) catalytic reduction of the latter proceeds via one-electron cleavage of the carbon-bromine bond to form a radical intermediate that undergoes cyclization to afford the substituted tetrahydrofurans.

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