Cas 386285-86-5,1-(ethoxymethylidene)amino-2-α,α,α-trifluoro-o-tolyl-4-ferrocenylmethylideneimidazolin-5-one

386285-86-5

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Basic information

Product Name: 1-(ethoxymethylidene)amino-2-α,α,α-trifluoro-o-tolyl-4-ferrocenylmethylideneimidazolin-5-one
Synonyms:
CAS NO:386285-86-5
Molecular Formula:
Molecular Weight: 510.299
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(ethoxymethylidene)amino-2-α,α,α-trifluoro-o-tolyl-4-ferrocenylmethylideneimidazolin-5-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(ethoxymethylidene)amino-2-α,α,α-trifluoro-o-tolyl-4-ferrocenylmethylideneimidazolin-5-one(386285-86-5)
EPA Substance Registry System: 1-(ethoxymethylidene)amino-2-α,α,α-trifluoro-o-tolyl-4-ferrocenylmethylideneimidazolin-5-one(386285-86-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 386285-86-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 386285-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,6,2,8 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 386285-86:
(8*3)+(7*8)+(6*6)+(5*2)+(4*8)+(3*5)+(2*8)+(1*6)=195
195 % 10 = 5
So 386285-86-5 is a valid CAS Registry Number.

386285-86-5Upstream product

386285-86-5Downstream Products

386285-86-5Relevant academic research and scientific papers

An efficient iminophosphorane-mediated synthesis, NMR-IR spectroscopic and X-ray study of novel ferrocenylimidazole derivatives: Part 10. Study on ferrocenes

Túrós, Gy?rgy,Csámpai, Antal,Czugler, Mátyás,Wamhoff, Heinrich,Sohár, Pál

, p. 122 - 130 (2001)

Starting from ethyl β-ferrocenyl-α-azidoacrylate (2), a series of novel 4-ferrocenylidene-1-aminoimidazolones (6a-j) was prepared in a pathway involving an aza-Wittig reaction followed by condensation of the resulting carbodiimidoester with hydrazines. Fo

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