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Isoxazole, 5-[1,1'-biphenyl]-4-yl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84864-17-5

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84864-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84864-17-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,6 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84864-17:
(7*8)+(6*4)+(5*8)+(4*6)+(3*4)+(2*1)+(1*7)=165
165 % 10 = 5
So 84864-17-5 is a valid CAS Registry Number.

84864-17-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-([1,1'-biphenyl]-4-yl)-isoxazole

1.2 Other means of identification

Product number -
Other names 5-[(1,1'-biphenyl)-4-yl]-isoxazole

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:84864-17-5 SDS

84864-17-5Relevant academic research and scientific papers

Preparation method of isoxazole derivative

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Paragraph 0048-0053, (2019/12/02)

The invention relates to a preparation method of an isoxazole derivative, which comprises the following steps of mixing an propargyl alcohol derivative, a halogen source, an acid and a solvent, and heating to react; adding the hydroxylamine into the react

Harnessing Stereospecific Z-Enamides through Silver-Free Cp?Rh(III) Catalysis by Using Isoxazoles as Masked Electrophiles

Debbarma, Suvankar,Bera, Sourav Sekhar,Maji, Modhu Sudan

supporting information, p. 835 - 839 (2019/01/26)

The stereospecific synthesis of Z-enamides is described in this paper. For the first time, isoxazoles have been employed as electrophiles in C-H functionalization to afford thermodynamically less stable Z-enamides utilizing salicylaldehydes in an atom- and step-economic fashion. The stereochemistry of enamides might originate from the relative disposition of atoms present in isoxazole and the intramolecular hydrogen bonding. The reaction showed excellent scope as several structurally and electronically diverse salicylaldehydes and isoxazoles reacted efficiently.

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