Cas 67705-42-4,1,4,7,10-tetrazatricyclo[5.5.1.0]tridecane

67705-42-4

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Basic information

Product Name: 1,4,7,10-tetrazatricyclo[5.5.1.0]tridecane
Synonyms:
CAS NO:67705-42-4
Molecular Formula:
Molecular Weight: 182.269
EINECS: N/A
Product Categories: N/A
Mol File: 67705-42-4.mol
Article Data: 7

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-tetrazatricyclo[5.5.1.0]tridecane(CAS DataBase Reference)
NIST Chemistry Reference: 1,4,7,10-tetrazatricyclo[5.5.1.0]tridecane(67705-42-4)
EPA Substance Registry System: 1,4,7,10-tetrazatricyclo[5.5.1.0]tridecane(67705-42-4)

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: 67705-42-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 67705-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,0 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67705-42:
(7*6)+(6*7)+(5*7)+(4*0)+(3*5)+(2*4)+(1*2)=144
144 % 10 = 4
So 67705-42-4 is a valid CAS Registry Number.

67705-42-4Upstream product

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67705-42-4Relevant articles and documents

A four-nitrogen [...] complex and its preparation method and application (by machine translation)

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Paragraph 0089; 0090; 0091, (2019/03/15)

The invention of the formula (D) compound and its preparation method. In particular, the present invention of the formula (D) illustrated compound and its use in preparing test cloth qu gai. The preparation method of the raw materials are easy, low cost, simple process, is conducive to industrial production, and compared with the existing method, in the course of preparing resin consumption is remarkably reduced, and has good application prospect. (by machine translation)

Non-cytotoxic, bifunctional EuIII and TbIII luminescent macrocyclic complexes for luminescence resonant energy-transfer experiments

Ferrand, Anne-Claire,Imbert, Daniel,Chauvin, Anne-Sophie,Vandevyver, Caroline D. B.,Buenzli, Jean-Claude G.

, p. 8678 - 8687 (2008/09/16)

A new macrocyclic ligand, L3, has been synthesised, based on the cyclen framework grafted with three phenacyl light-harvesting groups and a C5-alkyl chain bearing a carboxylic acid function as a potential linker for biological material. Acidity

Gadolinium DO3A derivatives mimicking phospholipids; preparation and in vitro evaluation as pH responsive MRI contrast agents

Hovland,Gl?ga?rd,Aasen,Klaveness

, p. 929 - 933 (2007/10/03)

A series of Gd-DO3A derivatives (8a-d) mimicking phospholipids have been prepared. Two of the complexes, Gd-HADB-DO3A (8a) and Gd-HADO-DO3A (8b), have been evaluated as pH responsive MRI contrast agents in vitro. The T1-relaxivity (r1/sub

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