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176-69-2

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176-69-2 Usage

General Description

2-Oxa-8-azaspiro[4.5]decane, also known as oxotremorine, is a chemical compound belonging to the class of spiro compounds. It is a heterocyclic compound with a spiro[decane-2,8'-imidazolidino] core structure. Oxotremorine is known for its pharmacological effects, particularly its ability to act as a muscarinic receptor agonist, meaning it can bind to and activate certain receptors in the body. 2-Oxa-8-azaspiro[4.5]decane has been studied for its potential use in the treatment of various conditions, including Alzheimer's disease, Parkinson's disease, and certain cognitive disorders. Its structure and pharmacological properties make it a subject of interest in medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 176-69-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,7 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 176-69:
(5*1)+(4*7)+(3*6)+(2*6)+(1*9)=72
72 % 10 = 2
So 176-69-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO/c1-4-9-5-2-8(1)3-6-10-7-8/h9H,1-7H2

176-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Oxa-8-azaspiro[4.5]decane

1.2 Other means of identification

Product number -
Other names 2-oxa-8-azaspiro[4,5]decane

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:176-69-2 SDS

176-69-2Relevant articles and documents

SELF-IMMOLATIVE LINKERS CONTAINING MANDELIC ACID DERIVATIVES, DRUG-LIGAND CONJUGATES FOR TARGETED THERAPIES AND USES THEREOF

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Page/Page column 70; 132; 133, (2015/03/28)

The invention provides a therapeutic drug and targeting conjugate, pharmaceutical compositions containing these conjugates in pharmaceutical composition, and uses of these conjugates in anti-neoplastic and other therapeutic regimens. Also provided are novel intermediates thereof. The conjugates provide a therapeutic drug fragment or prodrug fragment bound to a targeting moiety via a linker which comprises a substrate cleavable by a protease such as Cathepsin B. The targeting moiety is a ligand which targets a cell surface molecule, such as a cell surface receptor on an anti-neoplastic cell. The ligand may function solely as a targeting moiety or may itself have a therapeutic effect. Following administration of the therapeutic drug and targeting conjugate of formula I and exposure of the conjugate to the protease specific for the substrate, the linker is cleaved and the targeting moiety is separated from the conjugate, which causes the drug fragment or prodrug fragment to convert to the drug or prodrug. The recited conjugates are useful in anti-neoplastic therapies. Also provided are methods of making the therapeutic drug and targeting conjugates and intermediates thereof, and kits comprising the therapeutic drug and targeting conjugates.

Cyclohexane derivatives and their use as therapeutic agents

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Page 30, (2010/02/06)

The present invention relates compounds of formula (I), wherein ring A is a phenyl or pyridyl ring; X represents a linker selected from the group consisting of formulae: (a), (b), (c), (d), and (e); and R1, R2, R3, R4, R5, R6, R7, R13, R14, R15, R16, R17, R21a and R21b are as defined herein. The compounds are of particular use in the treatment or prevention of depression, anxiety, pain, inflammation, migraine, emesis or postherpetic neuralgia.

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