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2-(pyrrolidin-1-ylmethyl)naphthalen-1-ol is a chemical compound with a molecular formula C18H21NO. It is an organic compound that consists of a naphthalene ring attached to a pyrrolidine moiety. 2-(pyrrolidin-1-ylmethyl)naphthalen-1-ol also contains a hydroxyl group attached to the naphthalene ring. This chemical may be used in the synthesis of pharmaceuticals and other organic compounds. It possesses the potential to exhibit pharmacological properties, and it may have applications in the field of medicinal chemistry.

4931-36-6

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4931-36-6 Usage

Uses

Used in Pharmaceutical Synthesis:
2-(pyrrolidin-1-ylmethyl)naphthalen-1-ol is used as a key intermediate in the synthesis of various pharmaceuticals for its structural features that can be further functionalized to create new drug molecules.
Used in Medicinal Chemistry Research:
2-(pyrrolidin-1-ylmethyl)naphthalen-1-ol is used as a research compound in medicinal chemistry to explore its potential pharmacological properties and its role in the development of new therapeutic agents.
Used in Organic Chemistry:
2-(pyrrolidin-1-ylmethyl)naphthalen-1-ol is used as a building block in organic chemistry for the synthesis of complex organic molecules, taking advantage of its naphthalene and pyrrolidine moieties.
Further research and experimentation are necessary to fully understand the properties and potential uses of 2-(pyrrolidin-1-ylmethyl)naphthalen-1-ol.

Check Digit Verification of cas no

The CAS Registry Mumber 4931-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4931-36:
(6*4)+(5*9)+(4*3)+(3*1)+(2*3)+(1*6)=96
96 % 10 = 6
So 4931-36-6 is a valid CAS Registry Number.

4931-36-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Phenazine-2,3-diyldiamine

1.2 Other means of identification

Product number -
Other names 1,2-diaminopyridinium iodide

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:4931-36-6 SDS

4931-36-6Relevant academic research and scientific papers

IMIDAZOTRIAZINONE COMPOUNDS

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Paragraph 0750; 0751, (2013/10/08)

The present invention provides imidazotriazinone compounds which are inhibitors of phosphodiesterase 9 and pharmaceutically acceptable salt thereof. The present invention further provides processes, pharmaceutical compositions, pharmaceutical preparations and pharmaceutical use of the compounds in the treatment of PDE9 associated diseases or disorders in mammals, including humans.

NOVEL INHIBITOR COMPOUNDS OF PHOSPHODIESTERASE TYPE 10A

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, (2013/02/28)

The present invention relates to novel carboxamide compounds, pharmaceutical compositions containing them, and their use in therapy. The compounds possess valuable therapeutic properties and are particularly suitable for treating or controlling medical disorders selected from neurological disorders and psychiatric disorders, for ameliorating the symptoms associated with such disorders and for reducing the risk of such disorders

Piperazinylimidazopyridine and piperazinyltriazolopyridine antagonists of gonadotropin releasing hormone receptor

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Page/Page column 29; 41-42, (2008/06/13)

The present invention relates to Gonadotropin Releasing Hormone (GnRH, also known as Luteinizing Hormone Releasing Hormone) receptor antagonists.

Synthesis of Triazaphospholopyridines(1+)

Bansal, Raj K.,Gandhi, Neelam,Schmidpeter, A.,Karaghiosoff, K.

, p. 558 - 562 (2007/10/02)

Condensation of 1,2-diaminopyridinium iodides with tris(dimethylamino)phosphine gives triazaphospholopyridines 2a-d.Diethylamine adds to the N=P bond of 2a,b only if the phosphorus is oxidized at the same time.Hydrolysis of 2a opens the triazaphosphole ring at its 2,3-bond. - Keywords: 1,3-Diaza-2-phosphaindolizines, NMR Spectra, Mass Spectral Fragmentation, Hydrolysis, 1,2-Addition Reactions

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