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108392-50-3

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108392-50-3 Usage

Chemical Class

Diazabicyclo compounds

Explanation

The compound belongs to a class of bicyclic compounds containing two nitrogen atoms.

Explanation

The core structure of the compound consists of a six-membered ring with nitrogen atoms as part of the ring.

Explanation

The compound is a chlorinated derivative, meaning it has a chlorine atom added to the parent compound, 1,6-diazabicyclo[3.1.0]hexane.

Explanation

The compound contains a carboxamide group (-CONH2), a chloro group (-Cl), and an N-methyl group (-N(CH3)).

Explanation

The compound has specific stereochemistry at the 1, 5, and 6 positions of the ring, with the substituents being in the alpha configuration.

Explanation

The compound is used as a reagent to convert alcohols into mesylates or tosylates, which are important intermediates in organic chemistry.

Explanation

The compound acts as a catalyst to promote stereoselective cycloaddition reactions, which are crucial for the formation of complex molecular structures with specific stereochemistry.

Explanation

The compound can be used as a chiral base to facilitate enantioselective synthesis, which is the process of selectively producing one enantiomer of a chiral molecule over the other.

Explanation

Due to its unique structure and reactivity, the compound has potential applications in the development of new drugs and agrochemicals.

Explanation

The compound is registered with the 9CI (Chemical Abstracts Service) number, which is a unique identifier used in chemical databases.

Molecular Structure

Six-membered ring with two nitrogen atoms

Chlorinated Derivative

1,6-diazabicyclo[3.1.0]hexane

Functional Groups

Carboxamide, chloro, and N-methyl

Stereochemistry

(1-alpha-,5-alpha-,6-alpha-)

Application in Organic Synthesis

Reagent for alcohol conversion

Application in Organic Synthesis

Catalyst for stereoselective cycloaddition reactions

Application in Chiral Synthesis

Chiral base in enantioselective synthesis

Potential Applications

Pharmaceutical and agrochemical industries

Registry Number

9CI

Check Digit Verification of cas no

The CAS Registry Mumber 108392-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,9 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 108392-50:
(8*1)+(7*0)+(6*8)+(5*3)+(4*9)+(3*2)+(2*5)+(1*0)=123
123 % 10 = 3
So 108392-50-3 is a valid CAS Registry Number.

108392-50-3Relevant articles and documents

ASYMMETRICAL NITROGEN. 58. GEMINAL SYSTEMS. 37. N-CHLORODIAZIRIDINES

Shustov, G. V.,Denisenko, S. N.,Starovoitov, V. V.,Chervin, I. I.,Kostyanovskii, R. G.

, p. 1415 - 1421 (2007/10/02)

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