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Ethane-1,2-diamine - cobalt (3:1) is a coordination compound consisting of cobalt ions and ethane-1,2-diamine ligands. Ethane-1,2-diamine, also known as ethylenediamine, is a bidentate ligand with two nitrogen atoms that can form coordinate covalent bonds with metal ions. In this complex, three molecules of ethane-1,2-diamine are bonded to one cobalt ion, resulting in a 3:1 ratio. ethane-1,2-diamine - cobalt (3:1) is often used as a catalyst in various chemical reactions, particularly in the production of polyurethane foams and as a precursor in the synthesis of other cobalt complexes. The coordination geometry around the cobalt ion in this complex is typically octahedral, with the three ethane-1,2-diamine ligands occupying three of the six coordination sites.

7224-73-9

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7224-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7224-73-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,2 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7224-73:
(6*7)+(5*2)+(4*2)+(3*4)+(2*7)+(1*3)=89
89 % 10 = 9
So 7224-73-9 is a valid CAS Registry Number.

7224-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cobalt,ethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names N-isopentanoylglycine

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:7224-73-9 SDS

7224-73-9Downstream Products

7224-73-9Relevant academic research and scientific papers

Tandem intramolecular photocycloaddition-retro-mannich fragmentation as a route to spiro[pyrrolidine-3,3′-oxindoles]. Total synthesis of (±)-coerulescine, (±)-horsfiline, (±)-elacomine, and (±)-6-deoxyelacomine

White, James D.,Li, Yang,Ihle, David C.

experimental part, p. 3569 - 3577 (2010/07/04)

Figure presented Irradiation of a tryptamine linked through its side-chain nitrogen to an alkylidene malonate residue results in an intramolecular [2 + 2] cycloaddition to the indole 2,3-double bond. The resultant cyclobutane undergoes spontaneous retro-M

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