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2-Thiophenecarboxamide,3-fluoro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83933-19-1

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83933-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83933-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,3 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83933-19:
(7*8)+(6*3)+(5*9)+(4*3)+(3*3)+(2*1)+(1*9)=151
151 % 10 = 1
So 83933-19-1 is a valid CAS Registry Number.

83933-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-fluorothiophen-2-carboxamide

1.2 Other means of identification

Product number -
Other names 3-Fluoro-thiophene-2-carboxylic acid amide

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:83933-19-1 SDS

83933-19-1Downstream Products

83933-19-1Relevant academic research and scientific papers

SUBSTITUTED OXOPYRIDINE DERIVATIVES

-

Paragraph 0511-0514, (2018/05/24)

The invention relates to substituted oxopyridine derivatives and to processes for preparation thereof, and also to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially of cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

Protonation of Some 3-, 4-, and 5-Substituted Thiophen-2-carboxamides

Alberghina, Gaetano,Fisichella, Salvatore,Occhipinti, Salvatore,Consiglio, Giovanni,Spinelli, Domenico,Noto, Renato

, p. 1223 - 1226 (2007/10/02)

The protonation behaviour at 25 deg C in aqueous sulphuric acid solution of some 3-, 4-, and 5-substituted thiophen-2-carboxamides has been investigated by u.v. spectrophotometry. pKBH+ Values were calculated by HA and Bunnett-Olsen methods using the multivariate analysis.A positive ?α-s value was obtained indicating that the sulphur atom acts as an electron-withdrawing substituent.Plots of pKBH+of 4- and 5-substituted thiophen-2-carboxamides and 3-substituted derivatives against ? were linear with the slope +1.10 and +1.28, respectively.A ρo/ρm,p ratio higher than unity (1.16) has been observed indicating a larger transmission of electronic effects between the 2- and 3-positions of the thiophen ring than between the 2- and 4- or 5-positions.

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