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67321-81-7

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67321-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67321-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,2 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67321-81:
(7*6)+(6*7)+(5*3)+(4*2)+(3*1)+(2*8)+(1*1)=127
127 % 10 = 7
So 67321-81-7 is a valid CAS Registry Number.

67321-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Oxygen-17O2

1.2 Other means of identification

Product number -
Other names Benzene,1,3-dimethyl-,osmium complex

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:67321-81-7 SDS

67321-81-7Relevant articles and documents

Structure-function relationships for electrocatalytic water oxidation by molecular [Mn12O12] clusters

Yan, Yong,Lee, John S.,Ruddy, Daniel A.

supporting information, p. 4550 - 4555 (2015/05/20)

A series of Mn12O12(OAc)16-xLx(H2O)4 molecular clusters (L = acetate, benzoate, benzenesulfonate, diphenylphosphonate, dichloroacetate) were electrocatalytically investigated as water oxidation electrocatalysts on a fluorine-doped tin oxide glass electrode. Four of the [Mn12O12] compounds demonstrated water oxidation activity at pH 7.0 at varying overpotentials (640-820 mV at 0.2 mA/cm2) and with high Faradaic efficiency (85-93%). For the most active complex, more than 200 turnovers were observed after 5 min. Two structure-function relationships for these complexes were developed. First, these complexes must undergo at least one-electron oxidation to become active catalysts, and complexes that cannot be oxidized in this potential window were inactive. Second, a greater degree of distortion at Mn1 and Mn3 centers correlated with higher catalytic activity. From this distortion analysis, either or both of these two Mn centers are proposed to be the catalytically active site.

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