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2,7-Diazaspiro[4.4]nonane-2-carboxylic acid, 7-(phenylMethyl)-, 1,1-diMethylethyl ester is a complex organic chemical compound characterized by a unique spiro structure with two nitrogen atoms in the ring. It features a 7-(phenylMethyl) group attached to the carboxylic acid and a 1,1-diMethylethyl ester group attached to the nitrogen atom, giving it a molecular formula of C20H33N3O2. This ester derivative may hold potential in pharmaceutical applications or as a building block for other organic molecules due to its distinctive structural and functional attributes.

1177266-41-9

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1177266-41-9 Usage

Uses

Used in Pharmaceutical Industry:
2,7-Diazaspiro[4.4]nonane-2-carboxylic acid, 7-(phenylMethyl)-, 1,1-diMethylethyl ester is used as a potential pharmaceutical compound for its unique spiro structure and functional groups, which may contribute to the development of new drugs or therapeutic agents. Its specific application in this industry would require further research and testing to determine its properties and efficacy.
Used in Organic Synthesis:
In the field of organic synthesis, 2,7-Diazaspiro[4.4]nonane-2-carboxylic acid, 7-(phenylMethyl)-, 1,1-diMethylethyl ester serves as a building block for the creation of other complex organic molecules. Its unique structure and functional groups make it a valuable intermediate in the synthesis of various chemical entities, potentially leading to the discovery of new materials or compounds with specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1177266-41-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,7,2,6 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1177266-41:
(9*1)+(8*1)+(7*7)+(6*7)+(5*2)+(4*6)+(3*6)+(2*4)+(1*1)=169
169 % 10 = 9
So 1177266-41-9 is a valid CAS Registry Number.

1177266-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 7-benzyl-2,7-diazaspiro[4.4]nonane-2-carboxylate

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:1177266-41-9 SDS

1177266-41-9Relevant academic research and scientific papers

ADAMANTANE DERIVATIVES FOR THE TREATMENT OF FILOVIRUS INFECTION

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Paragraph 0886-0887, (2020/02/05)

Compounds of structural Formula I were developed for the treatment of infections by filoviruses including Ebolavirus and Marburgvirus, wherein, R1, R2, R3, X and Y are defined in the specification.

ADAMATANE DERIVATIVES FOR THE TREATMENT OF FILOVIRUS INFECTION

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Page/Page column 85, (2017/09/02)

Compounds of structural Formula (I) were developed for the treatment of infections by filoviruses including Ebolavirus and Marburgvirus.

SPIRODIAMINE-DIARYL KETOXIME DERIVATIVE

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Page/Page column 20, (2011/04/18)

[Problem] To provide a melanin concentrating hormone receptor antagonist useful as medicines for central system disorders, cardiovascular disorders, metabolic disorders. [Means for Resolution] Provided are compound of a formula (I): [wherein R1 a and R1 b each are a hydrogen atom, etc.; R2 is a hydrogen atom, a C1-6 alkyl, etc.; Ar1 is a 6-membered aromatic carbocyclic group or a 6-membered aromatic nitrogen-containing heterocyclic group; Ar2 is a group to be formed by removing two hydrogen atoms from a 6-membered aromatic carbon ring, a 6-membered aromatic nitrogen-containing hetero ring, etc.; Ar3 is a mono- or bi-cyclic aromatic carbon ring or aromatic hetero ring; m1, m2, m3 and m4 each are independently 0, 1, 2, 3 or 4, provided that the total of m1 and m2 is from 2 to 6, the total of m3 and m4 is from 2 to 6]. The compounds are useful as medicines for central system disorders, cardiovascular disorders, metabolic disorders.

Preparation and characterization of N-(3-pyridinyl) spirocyclic diamines as ligands for nicotinic acetylcholine receptors

Sippy, Kevin B.,Anderson, David J.,Bunnelle, William H.,Hutchins, Charles W.,Schrimpf, Michael R.

scheme or table, p. 1682 - 1685 (2009/11/30)

Several N-pyridin-3-yl spirobicyclic diamines, designed as conformationally restricted analogs of tebanicline (ABT-594), were synthesized as novel ligands for nicotinic acetylcholine receptors (nAChR). The spirocyclic compounds exhibited weaker binding affinity, than other constrained analogs in accord with a pharmacophore model. Nevertheless, some (1a, 1b) possessed (partial) agonist potencies comparable to nicotine at the α4β2 subtype, but with greatly improved selectivity relative to the α3β4* nAChR.

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