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4-carboxamidopiperidine-N-dithiocarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95480-31-2

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95480-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95480-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,4,8 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95480-31:
(7*9)+(6*5)+(5*4)+(4*8)+(3*0)+(2*3)+(1*1)=152
152 % 10 = 2
So 95480-31-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2OS2/c8-6(10)5-1-3-9(4-2-5)7(11)12/h5H,1-4H2,(H2,8,10)(H,11,12)

95480-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-carbamoylpiperidine-1-carbodithioic acid

1.2 Other means of identification

Product number -
Other names 4-Carboxyamidopiperidine-N-dithiocarbamate

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:95480-31-2 SDS

95480-31-2Downstream Products

95480-31-2Relevant academic research and scientific papers

Synthesis, characterization, HOMO-LUMO study, and antimicrobial activity of organotin(IV) complexes of 4-piperidine carboxamide and its Schiff base

Rizwan, Muhammad,Ali, Saqib,Shahzadi, Saira,Sharma, Saroj K.,Qanungo, Kushal,Shahid, Muhammad,Mahmood, Sohail

, p. 341 - 351 (2014)

A series of organotin(IV) complexes has been synthesized by reacting 4-piperidine carboxamide with CS2 and R2SnCl 2/R3SnCl in 1: 1 M/L ratio at room temperature. The synthesized complexes were further treated with benzaldehyde to synthesize Schiff bases under stirring. All the complexes were characterized by elemental analysis, FT-IR, 1H and 13C NMR. FT-IR and semi-empirical study confirm the bidentate nature of ligand. The complexes exhibit four-coordinate geometry in solution. Thermodynamic parameters and molecular descriptors were calculated by using semi-empirical PM3 method. HOMO-LUMO calculations show that chlorodiorganotin complexes are more susceptible to nucleophilic attack when compared with triorganotin complexes. Negative heats of formation at 298 K demonstrate that 1, 4, and 7 are thermodynamically stable. The antimicrobial results have shown that complexes containing Schiff base exhibit significantly better activity compared to complexes with carboxamide derivatives. 2014

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