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(2E)-3-(4-phenoxyphenyl)-1-phenylprop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90811-87-3

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90811-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90811-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,1 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90811-87:
(7*9)+(6*0)+(5*8)+(4*1)+(3*1)+(2*8)+(1*7)=133
133 % 10 = 3
So 90811-87-3 is a valid CAS Registry Number.

90811-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(4-phenoxyphenyl)-1-phenylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 4-Phenoxychalcone

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:90811-87-3 SDS

90811-87-3Downstream Products

90811-87-3Relevant academic research and scientific papers

Efficient synthesis of chalcones by a solid base catalyst

Kantam, M.Lakshmi,Veda Prakash,Venkat Reddy

, p. 1971 - 1978 (2007/10/03)

A simple and efficient heterogeneous procedure has been developed for the synthesis of chalcones (α,β-unsaturated ketones) by the Claisen-Schmidt condensation between arylaldehydes and ketones using Mg-Al-OtBu hydrotalcite (HT-OtBu) as catalyst. Copyright Taylor & Francis, Inc.

Solution phase synthesis of a spiro[pyrrolidine-2,3'-oxindole] library via a three component 1,3-dipolar cycloaddition reaction

Fokas, Demosthenes,Ryan, William J.,Casebier, David S.,Coffen, David L.

, p. 2235 - 2238 (2007/10/03)

A combinatorial library of 26,500 spiro[pyrrolidine,-2,3-oxindoles] was prepared in a single-compound format by a facile intermolecular 1,3-dipolar cycloaddition. An azomethine ylide, generated by the decarboxylative condensation of an isatin 1 with an α-amino acid 2, was trapped by a transchalcone 3 to afford heterocycles of the general structure 4. The regio- and stereochemistry of a representative product was determined by single crystal X-ray structure.

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