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53872-19-8

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53872-19-8 Usage

Synthesis Reference(s)

Tetrahedron, 49, p. 5445, 1993 DOI: 10.1016/S0040-4020(01)87261-6Tetrahedron Letters, 27, p. 5559, 1986 DOI: 10.1016/S0040-4039(00)85265-X

Check Digit Verification of cas no

The CAS Registry Mumber 53872-19-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,7 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53872-19:
(7*5)+(6*3)+(5*8)+(4*7)+(3*2)+(2*1)+(1*9)=138
138 % 10 = 8
So 53872-19-8 is a valid CAS Registry Number.

53872-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-methoxy-2-phenyl-1,3-oxazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 4-carbomethoxy-5-methoxy-2-phenyloxazole

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:53872-19-8 SDS

53872-19-8Relevant articles and documents

Nickel(II)-catalyzed diastereoselective [3+2] cycloaddition of N-tosyl-aziridines and aldehydes via selective carbon-carbon bond cleavage

Wu, Xingxing,Li, Lei,Zhang, Junliang

, p. 7824 - 7826 (2011)

An efficient and mild Ni(ClO4)2-catalyzed [3+2] cycloaddition of N-tosylaziridines and aldehydes via C-C bond cleavage was developed. The cycloaddition reaction proceeds with high diastereoselectivity and regioselectivity leading to

RhII-catalyzed cycloadditions of carbomethoxy iodonium ylides

Batsila, Christina,Kostakis, George,Hadjiarapoglou, Lazaros P

, p. 5997 - 6000 (2007/10/03)

Carbomethoxy iodonium ylides, generated from methyl acetoacetate and methyl malonate, respectively, are exploited in synthesis of cyclopropanes, cyclopropenes as well as various heterocycles.

Rhodium-catalyzed heterocycloaddition route to 1,3-oxazoles as building blocks in natural products synthesis

Connell,Tebbe,Gangloff,Helquist,Akermark

, p. 5445 - 5459 (2007/10/02)

Rhodium(II) acetate serves as a catalyst for the heterocycloaddition reaction of diazodicarbonyl compounds with nitriles to give functionalized 1,3-oxazole derivatives in a simple one-step procedure. In particular, dimethyl diazomalonate undergoes this re

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