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(1R,4R)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane, commonly known as quinuclidine, is a bicyclic amine compound characterized by its unique stereochemistry and a nitrogen-containing ring. It features a benzyl group attached to the second carbon atom, which contributes to its diverse applications in the pharmaceutical and chemical industries. Quinuclidine serves as a catalyst in organic synthesis, a base in organic reactions, a ligand in metal-catalyzed reactions, and a precursor in the synthesis of various organic compounds, making it a valuable tool for chemists and researchers in the field of organic chemistry.

1024010-90-9

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1024010-90-9 Usage

Uses

Used in Pharmaceutical Industry:
(1R,4R)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane is used as a catalyst in organic synthesis for the development of pharmaceutical compounds. Its unique stereochemistry and nitrogen-containing ring enable it to facilitate various chemical reactions, leading to the production of new and innovative drugs.
Used in Chemical Industry:
(1R,4R)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane is used as a base in organic reactions for the synthesis of various organic compounds. Its bicyclic amine structure allows it to act as a strong base, promoting the formation of desired products in chemical reactions.
Used in Metal-Catalyzed Reactions:
(1R,4R)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane is used as a ligand in metal-catalyzed reactions, enhancing the efficiency and selectivity of these processes. Its ability to coordinate with metal centers makes it a useful component in the development of new catalytic systems for organic synthesis.
Used in Synthesis of Organic Compounds:
(1R,4R)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane is used as a precursor in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its versatile structure and reactivity make it a valuable building block for the creation of complex molecules with specific properties and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 1024010-90-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,4,0,1 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1024010-90:
(9*1)+(8*0)+(7*2)+(6*4)+(5*0)+(4*1)+(3*0)+(2*9)+(1*0)=69
69 % 10 = 9
So 1024010-90-9 is a valid CAS Registry Number.

1024010-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,4R)-2-benzyl-2,5-diazabicyclo[2.2.1]heptane-2HCl

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 -
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More Details:1024010-90-9 SDS

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