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67496-78-0

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67496-78-0 Usage

General Description

Quinuclidin-4-yl methanamine, also known as Quinuclidine-4-methylamine, is a type of organic compound derived from quinuclidine. This chemical is often used in the development of pharmaceuticals and other drug compounds due to its capacity to act as a ligand, a molecule that binds to a central atom to form a coordination complex. Its chemical formula is C8H16N2 and it falls under the category of nitrogen heterocyclic compounds. Despite the potential toxic health risks it might present, its applications in medicinal chemistry make it vital in the pharmaceutical field.

Check Digit Verification of cas no

The CAS Registry Mumber 67496-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,9 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67496-78:
(7*6)+(6*7)+(5*4)+(4*9)+(3*6)+(2*7)+(1*8)=180
180 % 10 = 0
So 67496-78-0 is a valid CAS Registry Number.
InChI:InChI=1S/C8H16N2/c9-7-8-1-4-10(5-2-8)6-3-8/h1-7,9H2

67496-78-0SDS

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 1-(1-Azabicyclo[2.2.2]oct-4-yl)methanamine

1.2 Other means of identification

Product number -
Other names 3-AMINOMETHYL-1,2,3,4-TETRAHYDROISOQUINOLINE

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:67496-78-0 SDS

67496-78-0Upstream product

67496-78-0Relevant articles and documents

PROGRANULIN MODULATORS AND METHODS OF USING THE SAME

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Paragraph 0869, (2020/12/30)

Provided herein are compounds that modulate progranulin and methods of using the compounds in progranulin-associated disorders, such as Frontotemporal dementia (FTD).

2′ Biaryl amides as novel and subtype selective M1 agonists. Part I: Identification, synthesis, and initial SAR

Budzik, Brian,Garzya, Vincenzo,Shi, Dongchuan,Foley, James J.,Rivero, Ralph A.,Langmead, Christopher J.,Watson, Jeannette,Wu, Zining,Forbes, Ian T.,Jin, Jian

body text, p. 3540 - 3544 (2010/08/22)

Biaryl amides were discovered as novel and subtype selective M1 muscarinic acetylcholine receptor agonists. The identification, synthesis, and initial structure-activity relationships that led to compounds 3j and 4c, possessing good M1 agonist potency and intrinsic activity, and subtype selectivity for M1 over M2-5, are described.

THIAZOLYL COMPOUNDS USEFUL AS KINASE INHIBITORS

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Page/Page column 55, (2008/12/04)

The invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof. The formula I thiazolyl compounds inhibit tyrosine kinase activity thereby making them useful as anticancer agents and for the treatment of Alzheimer's disease

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