Cas 18273-26-2,1,1,4,4-Cyclohexanetetramine, N,N,N',N',N'',N'',N''',N'''-octafluoro-

18273-26-2

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Basic information

Product Name: 1,1,4,4-Cyclohexanetetramine, N,N,N',N',N'',N'',N''',N'''-octafluoro-
Synonyms:
CAS NO:18273-26-2
Molecular Formula: C6H8F8N4
Molecular Weight: 288.144
EINECS: N/A
Product Categories: N/A
Mol File: 18273-26-2.mol

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: 1,1,4,4-Cyclohexanetetramine, N,N,N',N',N'',N'',N''',N'''-octafluoro-(CAS DataBase Reference)
NIST Chemistry Reference: 1,1,4,4-Cyclohexanetetramine, N,N,N',N',N'',N'',N''',N'''-octafluoro-(18273-26-2)
EPA Substance Registry System: 1,1,4,4-Cyclohexanetetramine, N,N,N',N',N'',N'',N''',N'''-octafluoro-(18273-26-2)

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: 18273-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 18273-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,7 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18273-26:
(7*1)+(6*8)+(5*2)+(4*7)+(3*3)+(2*2)+(1*6)=112
112 % 10 = 2
So 18273-26-2 is a valid CAS Registry Number.

18273-26-2Upstream product

637-88-7 1,4-Cyclohexanedione

18273-26-2Downstream Products

130190-86-2 N,N-difluoroaminobenzene

18273-26-2Relevant academic research and scientific papers

Triphenylmethyldifluoramine: A stable reagent for the synthesis of gem-bis(difluoramines)

Prakash, G. K. Surya,Etzkorn, Markus,Olah, George A.,Christe, Karl O.,Schneider, Stefan,Vij, Ashwani

, p. 1712 - 1713 (2002)

The conversion of ketones into geminal bis(difluoramines) can be achieved under mild two-phase reaction conditions by employing triphenylmethyldifluoramine as an in situ source of difluoramine.

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