Cas 94154-81-1,1,3,9-trimethyl-7-(2,3,5,6-tetramethylphenacyl)xanthinium toluene-p-sulphonate

94154-81-1

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Basic information

Product Name: 1,3,9-trimethyl-7-(2,3,5,6-tetramethylphenacyl)xanthinium toluene-p-sulphonate
Synonyms: 1,3,9-trimethyl-7-(2,3,5,6-tetramethylphenacyl)xanthinium toluene-p-sulphonate
CAS NO:94154-81-1
Molecular Formula:
Molecular Weight: 540.64
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: 1,3,9-trimethyl-7-(2,3,5,6-tetramethylphenacyl)xanthinium toluene-p-sulphonate(CAS DataBase Reference)
NIST Chemistry Reference: 1,3,9-trimethyl-7-(2,3,5,6-tetramethylphenacyl)xanthinium toluene-p-sulphonate(94154-81-1)
EPA Substance Registry System: 1,3,9-trimethyl-7-(2,3,5,6-tetramethylphenacyl)xanthinium toluene-p-sulphonate(94154-81-1)

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: 94154-81-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 94154-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,5 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 94154-81:
(7*9)+(6*4)+(5*1)+(4*5)+(3*4)+(2*8)+(1*1)=141
141 % 10 = 1
So 94154-81-1 is a valid CAS Registry Number.

94154-81-1Upstream product

94154-81-1Downstream Products

94154-81-1Relevant academic research and scientific papers

Reactions of Xanthinium N(7)-Ylides with Olefinic Dipolarophiles

Hori, Mikio,Kataoka, Tadashi,Shimizu, Hiroshi,Imai, Eiji,Matsumoto, Yukiharu,et al.

, p. 1211 - 1220 (2007/10/02)

The stereo- and regio-chemical aspects of the reactions of xanthinium N(7)-methylides (2) with olefinic dipolarophiles were elucidated.The reactions of ylides (2) with N-phenylmaleimide afforded stereoselective endo adducts, and with acrylates and acrylon

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