41619-71-0

Basic information

• Product Name: COBALT, [[2,2'-[1,2-ETHANEDIYLBIS[(NITRILO-KN)METHYLIDYNE]]BIS[6-METHOXYPHENOLATO-KO]](2-)]-, (SP-4-2)-
• Synonyms: COBALT, [[2,2'-[1,2-ETHANEDIYLBIS[(NITRILO-KN)METHYLIDYNE]]BIS[6-METHOXYPHENOLATO-KO]](2-)]-, (SP-4-2)-;MeO-Salen-Co;COBALT,[[2,2''-[1,2-ETHANEDIYLBIS[(NITRILO-KN)METHYLIDYNE]]BIS[6-METHOXYPHENOLATO-KO]](2-)];(SP-4-2)-[[2,2'-[1,2-Ethanediylbis(nitrilomethylidyne)]bis[6-methoxyphenolato]](2-)-N2,N2',O1,O1']-cobalt;2,2'-[1,2-Ethanediylbis(nitrilomethylidyne)]bis[6-methoxyphenol] cobalt complex
• CAS NO: 41619-71-0
• Molecular Formula: C₁₈H₁₈CoN₂O₄
• Molecular Weight: 420.73
• Mol File: 41619-71-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: COBALT, [[2,2'-[1,2-ETHANEDIYLBIS[(NITRILO-KN)METHYLIDYNE]]BIS[6-METHOXYPHENOLATO-KO]](2-)]-, (SP-4-2)-(CAS DataBase Reference)
• NIST Chemistry Reference: COBALT, [[2,2'-[1,2-ETHANEDIYLBIS[(NITRILO-KN)METHYLIDYNE]]BIS[6-METHOXYPHENOLATO-KO]](2-)]-, (SP-4-2)-(41619-71-0)
• EPA Substance Registry System: COBALT, [[2,2'-[1,2-ETHANEDIYLBIS[(NITRILO-KN)METHYLIDYNE]]BIS[6-METHOXYPHENOLATO-KO]](2-)]-, (SP-4-2)-(41619-71-0)

Safety Data

• Hazardous Substances Data: 41619-71-0(Hazardous Substances Data)

Upstream product

• 7396-77-2 N,N'-bis(3-methoxysalicylidene)ethylenediamine 
• 6147-53-1 cobalt(II) diacetate tetrahydrate 
• 78166-97-9 2-hydroxy-3-methoxybenzaldehyde sodium salt 
• 18433-55-1 bis(2-hydroxy-3-methoxy-benzylidene)-ethylenediamine cobalt(II) monohydrate 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 

Relevant articles and documents

Syntheses of the Carotane-type Terpenoids (+)-Schisanwilsonene A and (+)-Tormesol via a Two-Stage Approach

Stereoselective syntheses of terpenoids in a more efficient manner have been a long-term pursuit for synthetic chemists. Herein we describe the two-step, enantiospecific and protecting-group-free synthesis of (+)-schisanwilsonene A from a carotane compound, which was produced in E. coli. We also completed the first enantiomeric synthesis of (+)-tormesol in five steps. The two-stage strategy offers a step- and redox-economical approach to prepare terpene natural products and their analogues.