Cas 1452849-45-4,N-benzyl-N',N''-ethylene-N-[(methoxycarbonyl)methyl]-N',N''-dimethylguanidinium hexafluorophosphate

1452849-45-4

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Basic information

Product Name: N-benzyl-N',N''-ethylene-N-[(methoxycarbonyl)methyl]-N',N''-dimethylguanidinium hexafluorophosphate
Synonyms: N-benzyl-N',N''-ethylene-N-[(methoxycarbonyl)methyl]-N',N''-dimethylguanidinium hexafluorophosphate
CAS NO:1452849-45-4
Molecular Formula:
Molecular Weight: 421.323
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: N-benzyl-N',N''-ethylene-N-[(methoxycarbonyl)methyl]-N',N''-dimethylguanidinium hexafluorophosphate(CAS DataBase Reference)
NIST Chemistry Reference: N-benzyl-N',N''-ethylene-N-[(methoxycarbonyl)methyl]-N',N''-dimethylguanidinium hexafluorophosphate(1452849-45-4)
EPA Substance Registry System: N-benzyl-N',N''-ethylene-N-[(methoxycarbonyl)methyl]-N',N''-dimethylguanidinium hexafluorophosphate(1452849-45-4)

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: 1452849-45-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1452849-45-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,2,8,4 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1452849-45:
(9*1)+(8*4)+(7*5)+(6*2)+(5*8)+(4*4)+(3*9)+(2*4)+(1*5)=184
184 % 10 = 4
So 1452849-45-4 is a valid CAS Registry Number.

1452849-45-4Upstream product

25653-11-6 2-(benzylimino)-1,3-dimethylimidazolidine

1452849-45-4Downstream Products

1452849-45-4Relevant academic research and scientific papers

Synthesis of the aziridinomitosene skeleton by application of guanidinium ylide-mediated aziridination

Kojima, Hiroyuki,Takahata, Chisato,Lemin, David,Takahashi, Masato,Kumamoto, Takuya,Nakanishi, Waka,Suzuki, Noriyuki,Ishikawa, Tsutomu

, p. 379 - 388 (2013/05/09)

An aziridinomitosene skeleton, a basic core of mitomycin antibiotics, was straightforwardly prepared from N-(p-toluenesulfonyl)indole-2-carboxaldehyde in 16% overall yield by successive reactions of guanidinium ylide-mediated aziridination, InCl3-catalyzed epimerization of trans-3-(indol-2-yl) aziridine-2-carboxylate, leading to the cis-derivative, and dehydrative cyclization. Copyright

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