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13820-78-5

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13820-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13820-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,2 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13820-78:
(7*1)+(6*3)+(5*8)+(4*2)+(3*0)+(2*7)+(1*8)=95
95 % 10 = 5
So 13820-78-5 is a valid CAS Registry Number.
InChI:InChI=1/3ClH.Co.4H3N.H2O/h3*1H;;4*1H3;1H2/q;;;+3;;;;;/p-3

13820-78-5SDS

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 azane,cobalt(3+),trichloride,hydrate

1.2 Other means of identification

Product number -
Other names Tetraammine(chloroaquo)cobalt(III)

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:13820-78-5 SDS

13820-78-5Downstream Products

13820-78-5Relevant articles and documents

Classic coordination complexes: The kinetics and stereochemistry of acid hydrolysis of cis- and trans-[Co(NH3)4Cl2]+

Jackson, W. Gregory

, p. 1955 - 1966 (2008/10/09)

The kinetics and stereochemistry of acid hydrolysis of the classic complexes cis- and trans-[Co(NH3)4Cl2]+ have been determined. They hydrolyse at virtually the same rate, 2.4 × 10-3 s-1 and 2.2 × 10-3 s-1 for the cis and trans ions, respectively, (0.02 M HClO4, 25 °C). The 'immeasurably fast' hydrolysis of the cis isomer has been dismissed as a myth. The trans-[Co(NH3)4(OH2)Cl]2+ isomer has been isolated for the first time, and the trans/cis isomerisation equilibration rate measured, again remarkably at virtually the same rate, 2.3 × 10-3 s-1. The cis isomer is the more stable at equilibrium, 88%. The steric course of substitution has been determined as 55% cis product for the cis-dichloro reactant and 35% cis for the trans reactant. The kinetic and equilibrium data are compared to that for the well-studied [Co(en)2Cl2]+ system, and the synthetic chemistry for the simpler tetraammine systems is elaborated.

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