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76790-97-1

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76790-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76790-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,9 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76790-97:
(7*7)+(6*6)+(5*7)+(4*9)+(3*0)+(2*9)+(1*7)=181
181 % 10 = 1
So 76790-97-1 is a valid CAS Registry Number.

76790-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetyl-3-oxobutanal,pentane-2,4-dione,ruthenium

1.2 Other means of identification

Product number -
Other names (3-formylpentane-2,4-dionato)bis(pentane-2,4-dionato)ruthenium(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:76790-97-1 SDS

76790-97-1Downstream Products

76790-97-1Relevant articles and documents

Rate-determining t2g-t2g electron transfer: Reaction of (3-formylpentane-2,4-dionato)bis(pentane-2,4-dionato)ruthenium(III) with titanium(III) and formation of (pentane-2,4-dionato)titanium(III)

Berrie, Barbara H.,Earley, Joseph E.

, p. 774 - 778 (2008/10/08)

The rate constants for the reaction of enol and keto forms of pentane-2,4-dione with Ti3+ (at 25°C in 1 M LiCl) are 2.4 × 103 M-1 s-1 and 0.7 M-1 s-1, respectively. (3-Formylpentane-2,4-dionato)bis(pentane-2,4-dionato)ruthenium(III) oxidizes Ti(III) in a reaction that involves two relaxations with rate constants kf′ ? k[Ti(III)]h[H+]-1 + k′ and ks′ ? 20 M-1 s-1, where h = [H+]/([H+] + 0.004 M), k = 2 × 102 M-1 s-1, and k′ = 750 M-1 s-1. These results are interpreted as indicating rate-determining electron transfer within a deprotonated binuclear intermediate.

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