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103440-75-1

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103440-75-1 Usage

General Description

4H-1-Benzopyran-4-one, 7-amino-2,3-dihydro- is a chemical compound with the molecular formula C10H11NO2. It is a derivative of 4H-1-benzopyran-4-one, a heterocyclic compound that consists of a pyran ring fused to a benzene ring. The compound contains an amino group and a dihydro moiety, which are important functional groups in organic chemistry. This chemical may have various applications in pharmaceuticals, agrochemicals, and other organic synthesis processes due to its unique structure and reactivity. Further research and study on this compound can provide insights into its potential uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 103440-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,4 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103440-75:
(8*1)+(7*0)+(6*3)+(5*4)+(4*4)+(3*0)+(2*7)+(1*5)=81
81 % 10 = 1
So 103440-75-1 is a valid CAS Registry Number.

103440-75-1SDS

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 7-Amino-2,3-dihydro-4H-chromen-4-one

1.2 Other means of identification

Product number -
Other names -

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:103440-75-1 SDS

103440-75-1Downstream Products

103440-75-1Relevant articles and documents

TYK2 INHIBITORS AND USES THEREOF

-

, (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.

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