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1,4-dibenzyl-6-hydroxymethyl-6-nitroperhydro-1,4-diazepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1173766-86-3

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1173766-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173766-86-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,7,6 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1173766-86:
(9*1)+(8*1)+(7*7)+(6*3)+(5*7)+(4*6)+(3*6)+(2*8)+(1*6)=183
183 % 10 = 3
So 1173766-86-3 is a valid CAS Registry Number.

1173766-86-3Relevant academic research and scientific papers

Fast and easy access to efficient bifunctional chelators for MRI applications

Gugliotta, Giuseppe,Botta, Mauro,Giovenzana, Giovanni Battista,Tei, Lorenzo

, p. 3442 - 3444 (2009)

Novel bifunctional agents based on the AAZTA (6-amino-6-methylperhydro-1,4-diazepinetetraacetic acid) structure with hydroxyl, carboxyl and chloro functional groups were prepared. The GdIII complexes show optimal magnetic properties making them

[Gd(AAZTA)]? Derivatives with n-Alkyl Acid Side Chains Show Improved Properties for Their Application as MRI Contrast Agents**

Kock, Flávio Vinicius Crizóstomo,Forgács, Attila,Guidolin, Nicol,Stefania, Rachele,Vágner, Adrienn,Gianolio, Eliana,Aime, Silvio,Baranyai, Zsolt

, p. 1849 - 1859 (2020/12/29)

Herein, the synthesis and an extensive characterization of two novel Gd(AAZTA) (AAZTA=6-amino-6-methylperhydro-1,4-diazepine tetra acetic acid) derivatives functionalized with short (C2 and C4) n-alkyl acid functions are reported. Th

Radiolabeled Dibenzodiazepinone-Type Antagonists Give Evidence of Dualsteric Binding at the M2 Muscarinic Acetylcholine Receptor

Pegoli, Andrea,She, Xueke,Wifling, David,Hübner, Harald,Bernhardt, Günther,Gmeiner, Peter,Keller, Max

supporting information, p. 3314 - 3334 (2017/05/05)

The dualsteric ligand approach, aiming at ligands with improved subtype selectivity, has been increasingly applied to muscarinic receptors (MRs). In this article, we present the synthesis and characterization of a M2R subtype-preferring radiola

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