Cas 873527-75-4,1,4,7,10-Tetraazacyclododecane-1,4,7-tricarboxylic acid, 10-(4-amino-2-nitrophenyl)-, tris(1,1-dimethylethyl) ester

873527-75-4

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Basic information

Product Name: 1,4,7,10-Tetraazacyclododecane-1,4,7-tricarboxylic acid, 10-(4-amino-2-nitrophenyl)-, tris(1,1-dimethylethyl) ester
Synonyms:
CAS NO:873527-75-4
Molecular Formula: C29H48N6O8
Molecular Weight: 608.736
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: 1,4,7,10-Tetraazacyclododecane-1,4,7-tricarboxylic acid, 10-(4-amino-2-nitrophenyl)-, tris(1,1-dimethylethyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: 1,4,7,10-Tetraazacyclododecane-1,4,7-tricarboxylic acid, 10-(4-amino-2-nitrophenyl)-, tris(1,1-dimethylethyl) ester(873527-75-4)
EPA Substance Registry System: 1,4,7,10-Tetraazacyclododecane-1,4,7-tricarboxylic acid, 10-(4-amino-2-nitrophenyl)-, tris(1,1-dimethylethyl) ester(873527-75-4)

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: 873527-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 873527-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,5,2 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 873527-75:
(8*8)+(7*7)+(6*3)+(5*5)+(4*2)+(3*7)+(2*7)+(1*5)=204
204 % 10 = 4
So 873527-75-4 is a valid CAS Registry Number.

873527-75-4Upstream product

873527-75-4Downstream Products

873527-80-1 10-[4-({1-methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-2-nitro-phenyl]-1,4,7,10tetraaza-cyclododecane-1,4,7-tricarboxylic acid tri-tert-butyl ester

873527-75-4Relevant academic research and scientific papers

Functionalized N-aryl-substituted cyclens by nucleophilic aromatic substitution

Subat, Michael,Gallmeier, Hans-Christoph,Fuchs, Andreas,Koenig, Burkhard

, p. 3003 - 3019 (2005)

The reaction of trifold protected cyclen with fluorinated dinitroarenes yields aryl-substituted or aryl-bridged cyclen derivatives in good yield. The two arene nitro groups, necessary for the nucleophilic aromatic substitution, are subsequently selectivel

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