Cas 446052-29-5,8-methyl-3-methoxycarbonyl-1,9-diphenyl-7-ethoxycarbonyl-4,6-dithia-1,2,9-triazaspiro[4.4]nona-2,7-diene

446052-29-5

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Basic information

Product Name: 8-methyl-3-methoxycarbonyl-1,9-diphenyl-7-ethoxycarbonyl-4,6-dithia-1,2,9-triazaspiro[4.4]nona-2,7-diene
Synonyms: 8-methyl-3-methoxycarbonyl-1,9-diphenyl-7-ethoxycarbonyl-4,6-dithia-1,2,9-triazaspiro[4.4]nona-2,7-diene
CAS NO:446052-29-5
Molecular Formula:
Molecular Weight: 455.558
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: 8-methyl-3-methoxycarbonyl-1,9-diphenyl-7-ethoxycarbonyl-4,6-dithia-1,2,9-triazaspiro[4.4]nona-2,7-diene(CAS DataBase Reference)
NIST Chemistry Reference: 8-methyl-3-methoxycarbonyl-1,9-diphenyl-7-ethoxycarbonyl-4,6-dithia-1,2,9-triazaspiro[4.4]nona-2,7-diene(446052-29-5)
EPA Substance Registry System: 8-methyl-3-methoxycarbonyl-1,9-diphenyl-7-ethoxycarbonyl-4,6-dithia-1,2,9-triazaspiro[4.4]nona-2,7-diene(446052-29-5)

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: 446052-29-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 446052-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,6,0,5 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 446052-29:
(8*4)+(7*4)+(6*6)+(5*0)+(4*5)+(3*2)+(2*2)+(1*9)=135
135 % 10 = 5
So 446052-29-5 is a valid CAS Registry Number.

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446052-29-5Relevant academic research and scientific papers

Heterocyclic thiones and their analogs in 1,3-dipolar cycloaddition: VII. Reaction of 4-methyl-1,3-thiazole-2(3H)-thiones with nitrile imines

Budarina,Dolgushina,Petrov,Labeish,Kol'Tsov,Bel'Skii

, p. 1516 - 1525 (2008/09/16)

Reactions of 4-methyl-1,3-thiazole-2(3H)-thiones with various C,N-disubstituted nitrile imines occurred by the common [3+2]-cycloaddition scheme leading to the formation in general of stable spiro compounds. In reactions of o-nitrophenylnitrile imines acy

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