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18778-81-9

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18778-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18778-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,7 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18778-81:
(7*1)+(6*8)+(5*7)+(4*7)+(3*8)+(2*8)+(1*1)=159
159 % 10 = 9
So 18778-81-9 is a valid CAS Registry Number.

18778-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-methyl-oxiranyl)-acrylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 4,5-Epoxy-2-hexensaeureethylester

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:18778-81-9 SDS

18778-81-9Upstream product

18778-81-9Downstream Products

18778-81-9Relevant articles and documents

Hydrocarbon oxidation catalyzed by manganese and iron complexes with the hexadentate ligand N,N′-di(ethylacetate)-N,N′-bis(2-pyridyl-methyl)- 1, 2-ethanediamine

Zhang, Qiao,Goldsmith, Christian R.

, p. 301 - 306 (2013/10/22)

Analogs of recently reported manganese and iron catalysts for alkene and alkane oxidation reactions have been prepared with the potentially hexadentate ligand N,N′-di(ethylacetate)-N,N′-bis(2-pyridylmethyl)-1, 2-ethanediamine (debpn). The Mn(II) and Fe(II) complexes, which were previously found to be hepta-coordinate in the solid state, are capable of catalyzing alkene epoxidation and aliphatic C-H activation reactions, although these activities are inferior to those of related complexes with less coordinating ligands. The hydrocarbon oxidation catalyzed by iron is more severely disrupted. Cyclic voltammetry indicates that the +2 oxidation states for both debpn complexes' metal ions are stabilized by the two additional chelate arms. Product analysis of the C-H activation and olefin epoxidation chemistries suggest that ligand-substrate steric interactions may exert additional inhibitory effects on the reactivity for the manganese catalysts.

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