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3-Thiophenecarboxamide, 2-amino-5-(2-fluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61019-15-6

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61019-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61019-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,1 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61019-15:
(7*6)+(6*1)+(5*0)+(4*1)+(3*9)+(2*1)+(1*5)=86
86 % 10 = 6
So 61019-15-6 is a valid CAS Registry Number.

61019-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-5-(2-fluorophenyl)thiophene-3-carboxamide

1.2 Other means of identification

Product number -
Other names 2-Amino-5-(2-fluorophenyl)-3-thiophene carboxamide

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:61019-15-6 SDS

61019-15-6Relevant academic research and scientific papers

Thiophene carboxamide inhibitors of JAK2 as potential treatments for myleoproliferative neoplasms

Haidle, Andrew M.,Zabierek, Anna A.,Childers, Kaleen K.,Rosenstein, Craig,Mathur, Anjili,Altman, Michael D.,Chan, Grace,Xu, Lin,Bachman, Eric,Mo, Jan-Rung,Bouthillette, Melaney,Rush, Thomas,Tempest, Paul,Marshall, C. Gary,Young, Jonathan R.

, p. 1968 - 1973 (2014/04/17)

A series of carboxamide-substituted thiophenes demonstrating inhibition of JAK2 is described. Development of this chemical series began with the bioisosteric replacement of a urea substituent by a pyridyl ring. Issues of chemical and metabolic stability were solved using the results of both in vitro and in vivo studies, ultimately delivering compounds such as 24 and 25 that performed well in an acute PK/PD model measuring p-STAT5 inhibition.

INHIBITORS OF JANUS KINASES

-

Page/Page column 72, (2009/01/23)

The instant invention provides for compounds that inhibit the four known mammalian JAK kinases (JAK1, JAK2, JAK3 and TYK2) and PDK1. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting the activity of JAK1, JAK2, JAK3 TYK2 and PDK1 by administering the compound to a patient in need of treatment for myeloproliferative disorders or cancer.

Nf-kb inhibitors

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, (2008/06/13)

The present invention provides novel compounds and methods for treating diseases with aminothiophene inhibitors of IKK-β phosphorylation of IκB.

Thiophene derivatives

-

, (2008/06/13)

Compounds of the formula: SPC1 Wherein R1 is NHR5 or OR5 where R5 is a hydrogen atom or alkyl group of 1-6 carbon atoms; R2 is a hydrogen atom or a CO.R6 group where R6 is an alk

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