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129-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129-67-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129-67:
(5*1)+(4*2)+(3*9)+(2*6)+(1*7)=59
59 % 10 = 9
So 129-67-9 is a valid CAS Registry Number.

129-67-9SDS

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 endothal-disodium

1.2 Other means of identification

Product number -
Other names disodium 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Herbicide
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:129-67-9 SDS

129-67-9Upstream product

129-67-9Downstream Products

129-67-9Relevant articles and documents

Crystal structures, DNA interaction and antiproliferative activities of the cobalt(II) and zinc(II) complexes of 2-amino-1,3,4-thiadiazole with demethylcantharate

Wang, Na,Lin, Qiu-Yue,Feng, Jie,Zhao, Yu-Ling,Wang, Yan-Jun,Li, Shi-Kun

experimental part, p. 3399 - 3406 (2011/01/11)

Two new mixed-ligand complexes [M(atdz)(DCA)(H2O) 2]·2H2O, (M = Co(II), Zn(II); atdz = 2-amino-1,3,4-thiadiazole, C2H3N3S; DCA = demethylcantharate, 7-oxabicyclo[2,2,1]heptane-2,3-dicarboxylate, C 8H8O5) were prepared and characterized by elemental analysis. The structures of the complexes were determined by X-ray diffraction. The crystals have empirical formulas CoC10H 19N3O9S (1) and ZnC10H 19N3O9S (2), respectively. Complex 1 and 2 are monoclinic systems with space group P21/m. The structures of the complexes assume severely distorted octahedral geometries. The DNA binding properties of the complexes were investigated by electronic absorption spectra, thermal denaturation studies, fluorescence quenching studies and viscosity measurements. All the results showed the interaction modes between the complexes and DNA were partial intercalation. The results of agarose gel electrophoresis indicated the complexes could cleave supercoiled DNA. The antiproliferative activities testing revealed that all the complexes showed weak to moderate activities against human hepatoma cells (SMMC7721) and human breast cells (MCF-7) in vitro.

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