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26163-74-6

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26163-74-6 Usage

General Description

The chemical "(E)-3-(2-furyl)-1-morpholin-4-yl-prop-2-en-1-one" is a molecule with a furan ring, a morpholine ring, and a propenone chain. It is also known as Furanone C-30 and is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. The furan ring provides aromaticity and stability to the molecule, while the morpholine ring and propenone chain contribute to its reactivity and potential biological activity. The molecule's chemical structure and functional groups make it a versatile building block for the synthesis of various complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 26163-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,6 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26163-74:
(7*2)+(6*6)+(5*1)+(4*6)+(3*3)+(2*7)+(1*4)=106
106 % 10 = 6
So 26163-74-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO3/c13-11(12-5-8-14-9-6-12)4-3-10-2-1-7-15-10/h1-4,7H,5-6,8-9H2/b4-3+

26163-74-6SDS

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-(furan-2-yl)-1-morpholin-4-ylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-(2-Furyl)acrylmorpholid

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:26163-74-6 SDS

26163-74-6Downstream Products

26163-74-6Relevant articles and documents

Structure-activity relationship of ortho- and meta-phenol based LFA-1 ICAM inhibitors

Lin, Edward Yin-Shiang,Guckian, Kevin M.,Silvian, Laura,Chin, Donovan,Ann Boriack-Sjodin,van Vlijmen, Herman,Friedman, Jessica E.,Scott, Daniel M.

scheme or table, p. 5245 - 5248 (2009/05/08)

LFA-1 ICAM inhibitors based on ortho- and meta-phenol templates were designed and synthesized by Mitsunobu chemistry. The selection of targets was guided by X-ray co-crystal data, and led to compounds which showed an up to 30-fold increase in potency over reference compound 1 in the LFA-1/ICAM1-Ig assay. The most active compound exploited a new hydrogen bond to the I-domain and exhibited subnanomolar potency.

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