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3-Benzyl-3-azaspiro[5.5]undecane is a complex organic compound with the molecular formula C17H29N. It features a spiro ring system, which consists of a nitrogen atom and a carbon atom connected to two different ring structures. The compound has a benzyl group attached to the nitrogen atom, which contributes to its unique chemical properties. This molecule is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and potential applications in pharmaceuticals or materials science. Its structure provides a foundation for further functionalization and exploration of its reactivity and potential uses.

4375-49-9

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4375-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4375-49-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4375-49:
(6*4)+(5*3)+(4*7)+(3*5)+(2*4)+(1*9)=99
99 % 10 = 9
So 4375-49-9 is a valid CAS Registry Number.

4375-49-9SDS

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 3-benzyl-3-azaspiro[5.5]undecane

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

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More Details:4375-49-9 SDS

4375-49-9Downstream Products

4375-49-9Relevant academic research and scientific papers

A hydrogen borrowing annulation strategy for the stereocontrolled synthesis of saturated aza-heterocycles

Armstrong, Roly J.,Chamberlain, Anna E. R.,Donohoe, Timothy J.,Paterson, Kieran J.,Twin, Heather C.

supporting information, p. 3563 - 3566 (2020/04/03)

An iridium catalyzed method for the synthesis of saturated aza-heterocycles from amines and diols is reported. A wide range of substituted heterocycles can be obtained using this approach including products bearing substituents at the C2, C3 and C4 positions. Employing water as the solvent, enantiopure diols could undergo annulation with minimal racemization, enabling the synthesis of valuable enantioenriched C3 and C4-substituted saturated aza-heterocycles.

SPIROPIPERIDINE COMPOUND AND MEDICINAL USE THEREOF

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Page/Page column 40, (2010/11/30)

The present invention relates to a CXCR3 antagonist comprising a compound represented by formula (I) (wherein all the symbols have the same meaning as defined in the description), a salt thereof, a quaternary ammonium salt thereof, an N-oxide form thereof or a solvate thereof, or a prodrug thereof. This antagonist is useful as a preventive, therapeutic and/or progression-suppressing agent for a CXCR3-mediated disease such as an immune or an allergic disease [e.g., an atopic disease, an autoimmune disease (e.g., multiple sclerosis, rheumatoid arthritis, systemic lupus erythematosus, type I diabetes, glomerulonephritis, Sjogren's syndrome and the like), systemic inflammatory response syndrome (SIRS), a rejection response to transplanted organ, tissue and/or cell or the like], a gastrointestinal disease [e.g., an inflammatory bowel disease or the like], or a respiratory disease [e.g., asthma, a chronic obstructive pulmonary disease or the like].

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