Cas 135672-52-5,1-Propanamine, 3-(2,3-dinitrophenoxy)-N,N-bis[3-(2,3-dinitrophenoxy)propyl]-

135672-52-5

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Basic information

Product Name: 1-Propanamine, 3-(2,3-dinitrophenoxy)-N,N-bis[3-(2,3-dinitrophenoxy)propyl]-
Synonyms:
CAS NO:135672-52-5
Molecular Formula: C27H27N7O15
Molecular Weight: 689.549
EINECS: N/A
Product Categories: N/A
Mol File: 135672-52-5.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-Propanamine, 3-(2,3-dinitrophenoxy)-N,N-bis[3-(2,3-dinitrophenoxy)propyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 1-Propanamine, 3-(2,3-dinitrophenoxy)-N,N-bis[3-(2,3-dinitrophenoxy)propyl]-(135672-52-5)
EPA Substance Registry System: 1-Propanamine, 3-(2,3-dinitrophenoxy)-N,N-bis[3-(2,3-dinitrophenoxy)propyl]-(135672-52-5)

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: 135672-52-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135672-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,7 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 135672-52:
(8*1)+(7*3)+(6*5)+(5*6)+(4*7)+(3*2)+(2*5)+(1*2)=135
135 % 10 = 5
So 135672-52-5 is a valid CAS Registry Number.

135672-52-5Upstream product

135672-52-5Downstream Products

135657-73-7 Tris<3-(2,3-diaminophenoxy)propyl>amin

135672-52-5Relevant academic research and scientific papers

Synthese von Di- und Tri(o-phenylendiamin)-Liganden

Hahn, Ekkehardt F.,Dittler-Klingemann, Andreas

, p. 779 - 782 (2007/10/02)

The o-phenylenediamine ligand trisamine, TRIPACEN (4) and bisamine, DIPACEN (8) are obtained by Williamson coupling of the potassium salt of 2,3-dinitrophenole (1) to tris(3-chlorpropyl)amine (2) or benzylbis(3-chlorpropyl)amine (5), respectively, followed by reduction of the nitro functions with Sn/HCl or Pd(OH)2/H2.

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