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2-methyl-2,3,3a,4,7,7a-hexahydro-1H-4,7-methanoisoindole is a complex organic compound with the molecular formula C11H15NO. It is a derivative of isoindole, which is a bicyclic aromatic compound consisting of a benzene ring fused to a pyrrolidine ring. The presence of a methyl group at the 2-position and a methano bridge between the 4 and 7 positions gives 2-methyl-2,3,3a,4,7,7a-hexahydro-1H-4,7-methanoisoindole its unique structure. This chemical is primarily of interest in the field of organic chemistry, particularly in the synthesis of various pharmaceuticals and other chemical compounds. Its hexahydro nature indicates that it contains six hydrogen atoms involved in hydrogen bonding, which can influence its physical and chemical properties. The compound's structure and properties make it a potential candidate for further study and application in the development of new materials and drugs.

6319-14-8

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6319-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6319-14-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6319-14:
(6*6)+(5*3)+(4*1)+(3*9)+(2*1)+(1*4)=88
88 % 10 = 8
So 6319-14-8 is a valid CAS Registry Number.

6319-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-2,3,3a,4,7,7a-hexahydro-1h-4,7-methanoisoindole

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

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More Details:6319-14-8 SDS

6319-14-8Relevant academic research and scientific papers

Enantioselective biocatalytic oxidative desymmetrization of substituted pyrrolidines

Koehler, Valentin,Bailey, Kevin R.,Znabet, Anass,Raftery, James,Helliwell, Madeleine,Turner, Nicholas J.

supporting information; body text, p. 2182 - 2184 (2010/06/18)

"Chemical Equation Presented" Center stage: Additions of nitrogen-centered radicals to cyanamide compounds provided the first radical synthesis of aromatic polycyclic guanidine derivatives (see scheme). Modular assembly of the substrates allows for a rapid increase of the molecular complexity of scaffolds, which have potential applications for medicinal chemistry.

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