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1,4,2-Dioxazole-5-acetic acid, 5-(methoxycarbonyl)-3-phenyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41931-34-4

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41931-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41931-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,3 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41931-34:
(7*4)+(6*1)+(5*9)+(4*3)+(3*1)+(2*3)+(1*4)=104
104 % 10 = 4
So 41931-34-4 is a valid CAS Registry Number.

41931-34-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxycarbonylmethyl-3-phenyl-[1,4,2]dioxazole-5-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names 5-Methoxycarbonylmethyl-3-phenyl-[1,4,2]dioxazole-5-carboxylic acid methyl ester

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:41931-34-4 SDS

41931-34-4Downstream Products

41931-34-4Relevant academic research and scientific papers

Vinylphosphonium Salt-Mediated Reactions: A One-Pot Condensation Approach for the Highly cis-Selective Synthesis of N-Benzoylaziridines and the Green Synthesis of 1,4,2-Dioxazoles as Two Important Classes of Heterocyclic Compounds

Aghahosseini, Hamideh,Ramazani, Ali,Jalayer, Nastaran Safarvand,Ranjdoost, Zahra,Souldozi, Ali,?lepokura, Katarzyna,Lis, Tadeusz

supporting information, p. 22 - 26 (2019/01/11)

An efficient, one-pot, and convenient approach for the reaction of the same precursors, trialkyl(aryl) phosphines, acetylene diesters, and benzhydroxamic acids has been developed to produce two important classes of heterocyclic compounds: N-benzoylaziridines and 1,4,2-dioxazoles. The strategy utilizes the intermediate solvation as a key step in product selectivity. The usefulness of the developed approach has been confirmed in the unprecedented highly cis-selective formation of the N-benzoylaziridines. In addition, the procedure provides a green alternative method for the synthesis of 1,4,2-dioxazoles employing a β-cyclodextrin nanoreactor in aqueous media.

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