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279-27-6

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279-27-6 Usage

Type of compound

bicyclic organic compound

Nitrogen atom

saturated bridgehead

State at room temperature

colorless liquid

Uses

commonly used as a precursor in the synthesis of various chemical compounds

Structure

fairly rigid and compact

Applications

useful in the design of pharmaceuticals, agrochemicals, and other specialty chemicals; used as a building block in the production of polymers and as a solvent in certain organic reactions; potential applications in the field of materials science

Additional

used as a strain energy benchmark in organic chemistry studies

Check Digit Verification of cas no

The CAS Registry Mumber 279-27-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 279-27:
(5*2)+(4*7)+(3*9)+(2*2)+(1*7)=76
76 % 10 = 6
So 279-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H11N/c1-3-7-4-2-6(1)5-7/h6H,1-5H2

279-27-6SDS

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 3-azabicyclo[2.2.1]heptane

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:279-27-6 SDS

279-27-6Relevant articles and documents

ELECTROLYTE, ELECTROLYTIC SOLUTION, AND ELECTROCHEMICAL DEVICE USING THE SAME

-

, (2010/04/30)

Disclosed herein is an electrolyte having excellent long-term reliability, a high withstanding voltage (a wide potential window), and high conductivity. The electrolyte contains a quaternary ammonium salt represented by the following general formula (1): wherein R1 represents a hydrocarbon group; R2 represents a hydrocarbon group, a hydrogen atom, or a halogen atom; R3 to R14 each represent an alkyl group, a fluoroalkyl group, a hydrogen atom or a halogen atom, C and C* each represent a carbon atom, N represents a nitrogen atom; h, i, j, x, y, and z are each an integer of 0 to 6, (h+x) is an integer of 0 to 6, (i+y) and (j+z) are each an integer of 1 to 6; and X? represents a counter anion having a HOMO energy of ?0.60 to ?0.20 a.u. as determined by the first-principle calculation on molecular orbital of the counter anion.

SPIRO-ISOXAZOLIDINE DERIVATIVES AS CHOLINERGIC AGENTS

-

, (2008/06/13)

Compounds of general formula I, STR1 wherein: A represents (CH. sub.2) m optionally substituted by R 3,B represents (CH. sub.2) n optionally substituted by R 4, R. sub.1 represents hydrogen, C 1-C 6 alkyl, C 1-6 alkenyl or C 1-6 alkynyl, R 2 represents hydrogen, C 1-C 6 alkyl or COOR 5, in which R 5 represents C 1-C 6 alkyl,R 3 and R. sub.4 independently represent hydrogen or C 1-C 6 alkyl, in addition, any two of R. sub.2, R 3 and R 4 may together form a C 1-3 alkylene chain,n and m independently represent an integer from 1-3 inclusive,Y represents O or S,and pharmaceutically acceptable acid addition salts thereof are useful as pharmaceuticals, in particular as central muscarinic acetylcholine receptor agonists. The compounds are therefore useful in the treatment of diseases such as presenile and senile dementia, Huntington's chorea, tardive dyskinesia, hyperkinesia, mania and Tourette Syndrome.

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