Cas 110886-16-3,2-Methyl-1-[1-(2-oxo-2-phenyl-ethylsulfanyl)-prop-(Z)-ylideneamino]-pyridinium; bromide

110886-16-3

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Basic information

Product Name: 2-Methyl-1-[1-(2-oxo-2-phenyl-ethylsulfanyl)-prop-(Z)-ylideneamino]-pyridinium; bromide
Synonyms: 2-Methyl-1-[1-(2-oxo-2-phenyl-ethylsulfanyl)-prop-(Z)-ylideneamino]-pyridinium; bromide
CAS NO:110886-16-3
Molecular Formula:
Molecular Weight: 379.321
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: 2-Methyl-1-[1-(2-oxo-2-phenyl-ethylsulfanyl)-prop-(Z)-ylideneamino]-pyridinium; bromide(CAS DataBase Reference)
NIST Chemistry Reference: 2-Methyl-1-[1-(2-oxo-2-phenyl-ethylsulfanyl)-prop-(Z)-ylideneamino]-pyridinium; bromide(110886-16-3)
EPA Substance Registry System: 2-Methyl-1-[1-(2-oxo-2-phenyl-ethylsulfanyl)-prop-(Z)-ylideneamino]-pyridinium; bromide(110886-16-3)

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: 110886-16-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110886-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,8 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110886-16:
(8*1)+(7*1)+(6*0)+(5*8)+(4*8)+(3*6)+(2*1)+(1*6)=113
113 % 10 = 3
So 110886-16-3 is a valid CAS Registry Number.

110886-16-3Upstream product

110886-16-3Downstream Products

110886-28-7 Thiobenzoic acid S-(2-ethyl-7-methyl-pyrazolo[1,5-a]pyridin-3-yl) ester

110886-16-3Relevant academic research and scientific papers

Preparation of New Nitrogen-Bridged Heterocycles. XIV. Further Investigation of the Desulfurization and the Rearrangement of Pyrido-1,3,4-thiadiazine Intermediates

Kakehi, Akikazu,Ito, Suketaka,Nagata, Kenji,Kinoshita, Naosumi,Kakinuma, Noboru

, p. 156 - 169 (2007/10/02)

The formation of pyrazolopyridine derivatives via the desulfurization and the rearrangement of pyrido-1,3,4-thiadiazine intermediates having various substituents at the 2- and 4-positions was investigated, and the wide applicability of this

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