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7-Nitro-4-chromanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22528-79-6

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22528-79-6 Usage

Chemical Properties

light yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 22528-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,2 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22528-79:
(7*2)+(6*2)+(5*5)+(4*2)+(3*8)+(2*7)+(1*9)=106
106 % 10 = 6
So 22528-79-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO4/c11-8-3-4-14-9-5-6(10(12)13)1-2-7(8)9/h1-2,5H,3-4H2

22528-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-nitro-2,3-dihydrochromen-4-one

1.2 Other means of identification

Product number -
Other names 7-Nitrochroman-4-one

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:22528-79-6 SDS

22528-79-6Downstream Products

22528-79-6Relevant academic research and scientific papers

TYK2 INHIBITORS AND USES THEREOF

-

Paragraph 0922; 0923; 0924, (2016/09/26)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

Sequential one-pot access to molecular diversity through aniline aqueous borylation

Erb, William,Albini, Mathieu,Rouden, Jacques,Blanchet, Jrme

, p. 10568 - 10580 (2015/01/08)

On the basis of our recently reported aniline aqueous borylation, molecular diversity was achieved in a one-pot process by combining other reactions such as esterification, Suzuki-Miyaura coupling, hydrogenolysis, or Petasis borono-Mannich.

An efficient synthesis of 4-chromanones

Zhong, Yong-Li,Boruta, David T.,Gauthier Jr., Donald R.,Askin, David

supporting information; experimental part, p. 4824 - 4826 (2011/10/04)

A two step efficient and practical synthesis of a variety of 4-chromanones is described. Phenols undergo a Michael addition to acrylonitriles in the presence of catalytic amounts of potassium carbonate and tert-butanol to generate the corresponding 3-aryloxypropanenitriles in 50-93% yields. Treatment of the resulting aryloxypropionitriles with 1.5 equiv of TfOH and 5 equiv of TFA, followed by an aqueous work up afforded 4-chromanones in moderate to excellent yields.

Substituted pyrazolyl compounds for the treatment of inflammation

-

, (2008/06/13)

The present invention relates to substituted pyrazolyl derivatives, compositions comprising such, intermediates, methods of making substituted pyrazolyl derivatives, and methods for treating cancer, inflammation, and inflammation-associated disorders, suc

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