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N-[Amino(imino)methyl]piperidine-1-carboximidamide is a complex organic compound with the chemical formula C8H16N4O. It is a derivative of piperidine, a heterocyclic amine, and features an imidamide functional group. N-[Amino(imino)methyl]piperidine-1-carboximidamide is characterized by the presence of an amino group attached to an imino group, which is in turn connected to a piperidine ring. The molecule also contains a carboximidamide group, which is a carbonyl group bonded to an imine. N-[Amino(imino)methyl]piperidine-1-carboximidamide is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other chemical products due to its unique structure and reactivity.

4705-40-2

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4705-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4705-40-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4705-40:
(6*4)+(5*7)+(4*0)+(3*5)+(2*4)+(1*0)=82
82 % 10 = 2
So 4705-40-2 is a valid CAS Registry Number.

4705-40-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (piperidine-1-carboximidoyl)-guanidine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4705-40-2 SDS

4705-40-2Relevant academic research and scientific papers

Synthesis and in Vitro AMPK Activation of Cycloalkyl/Alkarylbiguanides with Robust in Vivo Antihyperglycemic Action

Gutierrez-Lara, Erika,Martínez-Conde, Carlos,Rosales-Ortega, Edgar,Ramírez-Espinosa, Juan José,Rivera-Leyva, Julio C.,Centurión, David,Carvajal, Karla,Ortega-Cuellar, Daniel,Estrada-Soto, Samuel,Navarrete-Vázquez, Gabriel

, (2018/02/28)

This work describes the design, synthesis in one step, and the in vitro, in vivo, and in silico antidiabetic evaluation of a series of ten alicyclic and aromatic (alkyl +aryl: alkaryl)biguanides, analogues of metformin and phenformin. The design was conceived using isosteric replacement, chain-ring transformation, and lower and higher homologation strategies. All compounds were obtained as crystals and their structure was confirmed on the basis of their spectral data (NMR and mass spectra), and their purity was ascertained by microanalysis. Compounds were in vitro evaluated as activators of AMP-Activated Protein Kinase (AMPK). The results indicated that compounds 4, 5, and 6 showed similar or even better effect compared to metformin. Docking analysis was performed with regulatory subunit γ of AMPK, showing several interactions with nucleotide binding pocket. The in vivo evaluation of compounds 4-6 at a single dose of 50 mg/kg was performed in a murine experimental model of diabetes. The results showed an important and robust decrease of plasmatic glucose levels (-40%). Compound 6 was selected for an oral glucose tolerance test, showing an antihyperglycemic effect similar to metformin. The in vivo results indicated that compounds 4-6 may be effective in treating experimental T2DM.

3-deoxyglucosone and skin

-

, (2008/06/13)

The invention relates to a method of removing 3-deoxyglucosone and other alpha-dicarbonyl sugars from skin. The invention further relates to methods of inhibiting production and function of 3-deoxyglucosone and other alpha-dicarbonyl sugars in skin. The invention also relates to methods of treating 3-deoxyglucosone and other alpha-dicarbonyl sugars associated diseases and disorders of skin.

Biguanides and derivatives thereof as inhibitors of advanced glycosylation of a target protein

-

, (2008/06/13)

The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging). Accordingly, a composition is disclosed which comprises an agent capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with the carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation. The method comprises contacting the target protein with the composition. Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.

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