Cas 124548-24-9,[2-(2-Benzoyl-4,5-dimethoxy-phenyldisulfanyl)-4,5-dimethoxy-phenyl]-phenyl-methanone

124548-24-9

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Basic information

Product Name: [2-(2-Benzoyl-4,5-dimethoxy-phenyldisulfanyl)-4,5-dimethoxy-phenyl]-phenyl-methanone
Synonyms: [2-(2-Benzoyl-4,5-dimethoxy-phenyldisulfanyl)-4,5-dimethoxy-phenyl]-phenyl-methanone
CAS NO:124548-24-9
Molecular Formula:
Molecular Weight: 546.665
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-(2-Benzoyl-4,5-dimethoxy-phenyldisulfanyl)-4,5-dimethoxy-phenyl]-phenyl-methanone(CAS DataBase Reference)
NIST Chemistry Reference: [2-(2-Benzoyl-4,5-dimethoxy-phenyldisulfanyl)-4,5-dimethoxy-phenyl]-phenyl-methanone(124548-24-9)
EPA Substance Registry System: [2-(2-Benzoyl-4,5-dimethoxy-phenyldisulfanyl)-4,5-dimethoxy-phenyl]-phenyl-methanone(124548-24-9)

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: 124548-24-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124548-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,4 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 124548-24:
(8*1)+(7*2)+(6*4)+(5*5)+(4*4)+(3*8)+(2*2)+(1*4)=119
119 % 10 = 9
So 124548-24-9 is a valid CAS Registry Number.

124548-24-9Upstream product

124548-20-5 6,7-Dimethoxy-3-methyl-4-phenyl-2H-benzo[e][1,3]thiazin-3-ium; iodide

124548-24-9Downstream Products

124548-24-9Relevant academic research and scientific papers

Alkaline Hydrolysis of 3-Methyl-2H-1,3-benzothiazinium Iodides

Szabo, Janos,Bernath, Gabor,Sohar, Pal

, p. 789 - 791 (2007/10/02)

Alkaline hydrolysis of the 3-methyl-2H-1,3-benzothiazinium iodide 5a and of its 4-aryl derivatives 5b,c in the presence of hexacyanoferrate(III) ion resulted in the formation of 2,2'-diaryloxodiphenyl disulfides 6a-c.In contrast, the 4-benzyl derivative 5d underwent hydrogen iodide elimination to give the enamine 7.Mechanisms are proposed for the reactions.

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