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4264-05-5

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4264-05-5 Usage

Synthesis Reference(s)

Synthesis, p. 612, 1976 DOI: 10.1055/s-1976-24140

Check Digit Verification of cas no

The CAS Registry Mumber 4264-05-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4264-05:
(6*4)+(5*2)+(4*6)+(3*4)+(2*0)+(1*5)=75
75 % 10 = 5
So 4264-05-5 is a valid CAS Registry Number.

4264-05-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-nitrophenyl)-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 3-p-Nitrophenylisoxazole

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:4264-05-5 SDS

4264-05-5Relevant articles and documents

Polymer-supported vinyl sulfone as an efficient reagent for the synthesis of 3-monosubstituted isoxazoles

Wu, Guo-Jian,Sheng, Shou-Ri,Li, Dan,Xu, Li-Fan,Huang, Zhen-Zhong

, p. 3034 - 3043 (2013/09/12)

Polystyrene-supported vinyl sulfone reagent has been developed and used for solid-phase organic synthesis of 3-monosubstituted isoxazoles by 1,3-dipolar cycloaddition reaction with nitrile oxides and subsequent cleavage from the polymer support through an

Efficient and regioselective one-pot synthesis of 3-substituted and 3,5-disubstituted isoxazoles

Tang, Shibing,He, Jinmei,Sun, Yongquan,He, Liuer,She, Xuegong

supporting information; experimental part, p. 3982 - 3985 (2009/12/03)

(Figure Presented) A series of 3-substituted and 3,5-disubstituted isoxazoles have been efficiently synthesized in moderate to excellent yields by the reaction of N-hydroxyl-4-toluenesulfonamide with α,β-unsaturated aldehydes/ketones. This novel strategy is associated with readily available starting materials, mild conditions, high regioselectivity, and wide scope.

Substituent effects on 15N and 13C NMR chemical shifts of 3-phenylisoxazoles: A theoretical and spectroscopic study

Schofield, Mark H.,Sorel, Marie-Adele,Manalansan, Ryan J.,Richardson, David P.,Markgraf, J. Hodge

, p. 851 - 855 (2007/10/03)

The synthesis and assignment of 15N and 13C NMR signals of the isoxazole ring in a series of parasubstituted 3-phenyl derivatives are reported. DFT calculations of 15N and 13C chemical shifts are presented and c

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