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274712

Sigma-Aldrich

N,N′-Bis(salicylidene)ethylenediaminocobalt(II)

99%

Synonym(s):

Co(salen), N,N′-Disalicylidene-ethylenediamine cobalt(II) salt, Co(SALEN)2, Ethylenebis(salicylimine) cobalt(II) salt, Salcomine

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About This Item

Linear Formula:
[-CH2N=CHC6H4-2-(O-)]2Co
CAS Number:
14167-18-1
Molecular Weight:
325.23
EC Number:
238-012-5
MDL number:
MFCD00000009
UNSPSC Code:
12352300
PubChem Substance ID:
24856599

Assay

99%

reaction suitability

core: cobalt
reagent type: catalyst

SMILES string

C1C\N=C\c2ccccc2O[Co]Oc3ccccc3\C=N\1

InChI

1S/C16H16N2O2.Co/c19-15-7-3-1-5-13(15)11-17-9-10-18-12-14-6-2-4-8-16(14)20;/h1-8,11-12,19-20H,9-10H2;/q;+2/p-2/b17-11+,18-12+;

InChI key

NPAQSKHBTMUERN-OYJDLGDISA-L

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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S Watanabe et al.
Antiviral chemistry & chemotherapy, 9(3), 269-274 (1999-01-06)
Salcomine, N,N'-bis(salicylidene)ethylene diamino-cobalt (II), and its derivatives were evaluated for their ability to inhibit selectively human cytomegalovirus (HCMV) proteinase activity. The 50% inhibitory concentration (IC50) of salcomine was 1.4 microM for HCMV proteinase, but > 200 microM for three other
K Otsuji et al.
Advances in space research : the official journal of the Committee on Space Research (COSPAR), 7(4), 69-72 (1987-01-01)
Oxygen concentration and separation is an essential factor for air recycling in a CELSS. Furthermore, if the value of the plant assimilatory quotient is not coincident with that of the animal respiratory quotient, the recovery of O2 from the concentrated
Adushan Pillay et al.
Organic & biomolecular chemistry, 10(38), 7809-7819 (2012-08-24)
The synthesis of two closely related pyranonaphthoquinones, dehydroherbarin and anhydrofusarubin, is described. The construction of the naphthalene nuclei was achieved using the Stobbe condensation reaction using 2,4-dimethoxybenzaldehyde and 2,4,5-trimethoxybenzaldehyde as their respective starting materials. Two key steps en route include

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