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69306-90-7

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69306-90-7 Usage

Physical form

Yellow to orange powder

Use

Fungicide in agricultural applications

Application methods

Foliar spray or soil treatment

Mechanism of action

Inhibits growth and reproduction of fungal pathogens

Stability

Relatively stable

Toxicity

Low toxicity to non-target organisms

Popularity

Popular choice for controlling fungal diseases in agriculture

Check Digit Verification of cas no

The CAS Registry Mumber 69306-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,0 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69306-90:
(7*6)+(6*9)+(5*3)+(4*0)+(3*6)+(2*9)+(1*0)=147
147 % 10 = 7
So 69306-90-7 is a valid CAS Registry Number.

69306-90-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name copper,1H-pyrimidine-2-thione

1.2 Other means of identification

Product number -
Other names -

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:69306-90-7 SDS

69306-90-7Downstream Products

69306-90-7Relevant articles and documents

Probing the limits of steric constraints in the oligomerization of copper(I) complexes: Structures of two sterically congested oligomers

Wycliff, Christina,Bharathi, D. Saravana,Samuelson, Ashoka G.,Nethaji, Munirathinam

, p. 949 - 958 (2008/10/08)

Oligomeric copper(I) clusters are formed by the insertion reaction of copper(I) aryloxides into heterocumulenes. The effect of varying the steric demands of the heterocumulene and the aryloxy group on the nuclearity of the oligomers formed has been probed. Reactions with copper(I)2-methoxyphenoxide and copper(I)2-methylphenoxide with PhNCS result in the formation of hexameric complexes hexakis[N-phenylimino(aryloxy)methanethiolato copper(I)] 3 and 4 respectively. Single crystal X-ray data confirmed the structure of 3. Similar insertion reactions of CS2 with the copper(I) aryloxides formed by 2,6-di-tert-butyl-4-methylphenol and 2,6-dimethylphenol result in oligomeric copper(I) complexes 7 and 8 having the (aryloxy)thioxanthate ligand. Complex 7 was confirmed to be a tetramer from single crystal X-ray crystallography. Reactions carried out with 2-mercaptopyrimidine, which has ligating properties similar to N-alkylimino(aryloxy)methanethiolate, result in the formation of an insoluble polymeric complex 11. The fluorescence spectra of oligomeric complexes are helpful in determining their nuclearity. It has been shown that a decrease in the steric requirements of either the heterocumulene or aryloxy parts of the ligand can compensate for steric constraints and facilitate oligomerization.

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