Cas 124357-52-4,[6-(2-Hydroxy-ethyl)-2,5,8-trimethyl-8,8a,9,10-tetrahydro-7-thia-1,3,9,10a-tetraaza-anthracen-8-yl]-phenyl-methanone

124357-52-4

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Basic information

Product Name: [6-(2-Hydroxy-ethyl)-2,5,8-trimethyl-8,8a,9,10-tetrahydro-7-thia-1,3,9,10a-tetraaza-anthracen-8-yl]-phenyl-methanone
Synonyms:
CAS NO:124357-52-4
Molecular Formula:
Molecular Weight: 396.513
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: [6-(2-Hydroxy-ethyl)-2,5,8-trimethyl-8,8a,9,10-tetrahydro-7-thia-1,3,9,10a-tetraaza-anthracen-8-yl]-phenyl-methanone(CAS DataBase Reference)
NIST Chemistry Reference: [6-(2-Hydroxy-ethyl)-2,5,8-trimethyl-8,8a,9,10-tetrahydro-7-thia-1,3,9,10a-tetraaza-anthracen-8-yl]-phenyl-methanone(124357-52-4)
EPA Substance Registry System: [6-(2-Hydroxy-ethyl)-2,5,8-trimethyl-8,8a,9,10-tetrahydro-7-thia-1,3,9,10a-tetraaza-anthracen-8-yl]-phenyl-methanone(124357-52-4)

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: 124357-52-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124357-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,5 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 124357-52:
(8*1)+(7*2)+(6*4)+(5*3)+(4*5)+(3*7)+(2*5)+(1*2)=114
114 % 10 = 4
So 124357-52-4 is a valid CAS Registry Number.

124357-52-4Upstream product

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124357-52-4Relevant academic research and scientific papers

Novel S-Alkylation Products from "Isolated Thiamin Ylide" via Thiaminium Neothiaminthiolate Ion Pair

Sugimoto, Hirohiko,Ishiba, Teruyuki,Sato, Tomohiro,Nakai, Hiroshi,Hirai, Kentaro

, p. 467 - 470 (1990)

The ambident anion character of thiamin ylide was demonstrated by alkylation reactions of the "isolated thiamin ylide" under neutral or basic conditions.Alkylation with alkyl halides yielded S-alkyl derivatives of the yellow form of thiamin (pyrimidopyrimidine derivatives) instead of 2-alkylthiamin.These and previous results provide chemical evidence that thiamin ylide and thiaminium neothiaminthiolate (8) undergo a facile interconversion in EtOH.

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