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85003-78-7

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85003-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85003-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,0 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85003-78:
(7*8)+(6*5)+(5*0)+(4*0)+(3*3)+(2*7)+(1*8)=117
117 % 10 = 7
So 85003-78-7 is a valid CAS Registry Number.

85003-78-7SDS

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 6-(5-amino-3H-1,3,4-thiadiazol-2-ylidene)cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 2-(amino-[1,3,4]thiadiazol-2-yl)-phenol

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:85003-78-7 SDS

85003-78-7Relevant articles and documents

Synthesis and antifungal activities of 5-(o-hydroxy phenyl)-2-[4'aryl-3' chloro-2'azetidinon-1-yl]-1,3,4-thiadiazole

Gupta, Shiv K.,Sharma,Bansal,Kumar

, p. 594 - 597 (2011)

New series of 5-(o-hydroxy phenyl)-2-[4'aryl-3'chloro-2'azetidinon- 1-yl]-1,3,4-thiadiazole have been synthesized and the structures of the new compounds were established on the basis of IR, 1H NMR spectral data. In vitro antifungal activity (MIC activity) was evaluated and compared with standard drugs of ketoconazole. Compounds 3c in the series has shown interesting antifungal activity against both C. albicans and A. niger fungus. In the gratifying result, most of the compounds were found to have moderate antifungal activity.

Synthesis, characterization and biological activity study of some new metal complexes with schiff's bases derived from [o-vanillin] with [2-amino-5-(2-hydroxy-phenyl)-1,3,4-thiadiazole]

Shaalan, Naser,Mahdi, Shatha

, p. 4059 - 4067 (2021/07/31)

This study involves the preparation of a new series of dinuclear complexes Cr(III), Co(II), Ni(II), Cu(II) and Zn(II) complexes of the Schiff base (H2L) derived from Vanillin with 2amino-5-(2-hydroxy-phenyl)-1,3,4-thiadiazole has been synthesized tetradentate Schiff base ligands were used for complexation upon two metal ions of Cr(III),Co(II), Ni(II), Cu(II) and Zn(II) as dineucler formula M2L2.4H2O and M2L2. These ligands can be characterization IR ,UV-Vis , Mass, 1H-NMR and elemental microanalysis. The Synthesized complexes were characterized by IR, spectroscopy ,elemental microanalysis, electronic spectra, magnetic susceptibility conductive ,thermal Analysis (TGA) and atomic absorption on the basis of analytical data, the stoichiometry of metal to ligand in complexes and Schiff bases ligand. The Structures of complexes were proposed from the measurements. The bioactivity of the prepared complexes has been examined with antibacterial activity. Antimicrobial activities of the Schiff base ligand and their metal complexes reveal that the Schiff base transition metal complexes show significant activity against some fungi and bacteria.

Synthesis, in vitro and in silico Anti-Proliferative Studies of Novel Piperiene-Oxadiazole and Thiadiazole Analogs

Amperayani,Parimi

, p. 2301 - 2307 (2020/01/08)

Piperine is a component of pepper which has earlier been reported as anticancer active compound. This work is emphasized on the design and synthesis of new hybrid piperine analogs by coupling piperine with the amine group of oxadiazoles and thiadiazoles.

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