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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108392-50-3
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Basic information
- Product Name: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,6-chloro-N-methyl-,(1-alpha-,5-alpha-,6-alpha-)-(9CI)
- Synonyms: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,6-chloro-N-methyl-,(1-alpha-,5-alpha-,6-alpha-)-(9CI)
- CAS NO:108392-50-3
- Molecular Formula: C6H10ClN3O
- Molecular Weight: 0
- EINECS: N/A
- Product Categories: PYRROLE
- Mol File: 108392-50-3.mol
- Article Data: 2
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,6-chloro-N-methyl-,(1-alpha-,5-alpha-,6-alpha-)-(9CI)(CAS DataBase Reference)
- NIST Chemistry Reference: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,6-chloro-N-methyl-,(1-alpha-,5-alpha-,6-alpha-)-(9CI)(108392-50-3)
- EPA Substance Registry System: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,6-chloro-N-methyl-,(1-alpha-,5-alpha-,6-alpha-)-(9CI)(108392-50-3)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 108392-50-3(Hazardous Substances Data)
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108392-50-3 Usage
Chemical Class
Diazabicyclo compoundsExplanation
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 atomsChlorinated Derivative
1,6-diazabicyclo[3.1.0]hexaneFunctional Groups
Carboxamide, chloro, and N-methylStereochemistry
(1-alpha-,5-alpha-,6-alpha-)Application in Organic Synthesis
Reagent for alcohol conversionApplication in Organic Synthesis
Catalyst for stereoselective cycloaddition reactionsApplication in Chiral Synthesis
Chiral base in enantioselective synthesisPotential Applications
Pharmaceutical and agrochemical industriesRegistry Number
9CICheck 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.
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1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,6-chloro-N-methyl-,(1-alpha-,5-alpha-,6-alpha-)-(9CI)
