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87051-83-0

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87051-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87051-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,0,5 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87051-83:
(7*8)+(6*7)+(5*0)+(4*5)+(3*1)+(2*8)+(1*3)=140
140 % 10 = 0
So 87051-83-0 is a valid CAS Registry Number.

87051-83-0SDS

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-hydroxy-1,2-diphenylethylidene)amino]thiourea

1.2 Other means of identification

Product number -
Other names 2-hydroxy-2-phenylacetophenone thiosemicarbazone

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:87051-83-0 SDS

87051-83-0Relevant articles and documents

Spectroscopic and electrochemical characterization of some Schiff base metal complexes containing benzoin moiety

El-Shahawi,Al-Jahdali,Bashammakh,Al-Sibaai,Nassef

, p. 459 - 465 (2014/01/23)

(Graph Presented)The ligation behavior of bis-benzoin ethylenediamine (B2ED) and benzoin thiosemicarbazone (BTS) Schiff bases towards Ru3+, Rh3+, Pd2+, Ni2+ and Cu 2+ were determined. The b

Synthesis, anti-bacterial and anti-fungal activities of some novel Schiff bases containing 2,4-disubstituted thiazole ring

Bharti,Nath,Tilak,Singh

experimental part, p. 651 - 660 (2010/04/02)

A series of arylidene-2-(4-(4-methoxy/bromophenyl) thiazol-2-yl) hydrazines (4a-z) and 1-(4-(4-methoxy/bromophenyl) thiazol-2-yl)-2-cyclohexylidene/cyclopentylidene hydrazines (5a-b/6a-b) were synthesized, characterized and screened for their antimicrobial activities. The structures of synthesized compounds were established by spectroscopic (FT-IR, 1H NMR, 13C NMR, Mass) and elemental analyses. Both the anti-bacterial and anti-fungal activities with MIC values of compounds were evaluated. The results of anti-bacterial screening reveal that among all the compounds screened eight compounds showed moderate to good anti-bacterial activity while ten of the newly synthesized compounds displayed good to excellent anti-fungal activity. Among the tested compounds, the most effective compounds with MIC value in the range of 6.25-25 μg/ml are 4a, 4n, 4z, 5a, 5b, 6a and 6b against three fungal strains viz. Candida albicans, Cryptococcus neoformans and Aspergillus flavus.

Synthesis and spectral studies of platinum metal complexes of benzoin thiosemicarbazone

Offiong, Offiong E.

, p. 2167 - 2176 (2007/10/02)

The platinum metal chelates of benzoin thiosemicarbazone obtained with Ru(III), Rh(III), Ir(III), Pd(II) and Pt(II) were prepered from their corresponding halide salts.The complexes were characterized by elemental analysis, conductance measurement, IR, Ra

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