5182-90-1,MFCD01684982
Catalog No.:AA00DE4P

5182-90-1 | Quinoxaline-2-carboxamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$107.00   $75.00
- +
1g
98%
in stock  
$250.00   $175.00
- +
5g
98%
in stock  
$726.00   $508.00
- +
10g
98%
in stock  
$1,202.00   $842.00
- +
25g
98%
in stock  
$2,394.00 $1,676.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00DE4P
Chemical Name:
Quinoxaline-2-carboxamide
CAS Number:
5182-90-1
Molecular Formula:
C9H7N3O
Molecular Weight:
173.1714
MDL Number:
MFCD01684982
SMILES:
NC(=O)c1cnc2c(n1)cccc2
NSC Number:
90836
Properties
Properties
 
BP:
430.8°C at 760 mmHg  
Form:
Solid  
MP:
199-201℃  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
207  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1  

Literature

Title: 3-Carbamoylquinoxalin-1-ium chloride.

Journal: Acta crystallographica. Section E, Structure reports online 20120101

Title: Studies on log Po/w of quinoxaline di-N-oxides: a comparison of RP-HPLC experimental and predictive approaches.

Journal: Molecules (Basel, Switzerland) 20110913

Title: In silico quantitative structure-activity relationship studies on P-gp modulators of tetrahydroisoquinoline-ethyl-phenylamine series.

Journal: BMC structural biology 20110101

Title: Synthesis and antimycobacterial activity of new quinoxaline-2-carboxamide 1,4-di-N-oxide derivatives.

Journal: European journal of medicinal chemistry 20101001

Title: Structure-activity relationship (SAR) studies of quinoxalines as novel HCV NS5B RNA-dependent RNA polymerase inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20070315

Title: Synthesis and antimycobacterial activity of new quinoxaline-2-carboxamide 1,4-di-N-oxide derivatives.

Journal: Bioorganic & medicinal chemistry 20030515

Title: Synthesis and antimycobacterial activity of pyrazine and quinoxaline derivatives.

Journal: Journal of medicinal chemistry 20021205

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SDS
Tags:5182-90-1 Molecular Formula|5182-90-1 MDL|5182-90-1 SMILES|5182-90-1 Quinoxaline-2-carboxamide
Catalog No.: AA00DE4P
5182-90-1,MFCD01684982
5182-90-1 | Quinoxaline-2-carboxamide
Pack Size: 250mg
Purity: 98%
in stock
$107.00 $75.00
Pack Size: 1g
Purity: 98%
in stock
$250.00 $175.00
Pack Size: 5g
Purity: 98%
in stock
$726.00 $508.00
Pack Size: 10g
Purity: 98%
in stock
$1,202.00 $842.00
Pack Size: 25g
Purity: 98%
in stock
$2,394.00 $1,676.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00DE4P
Chemical Name: Quinoxaline-2-carboxamide
CAS Number: 5182-90-1
Molecular Formula: C9H7N3O
Molecular Weight: 173.1714
MDL Number: MFCD01684982
SMILES: NC(=O)c1cnc2c(n1)cccc2
NSC Number: 90836
Properties
BP: 430.8°C at 760 mmHg  
Form: Solid  
MP: 199-201℃  
Storage: Keep in dry area;Room Temperature;  
Complexity: 207  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1  
Literature fold

Title: 3-Carbamoylquinoxalin-1-ium chloride.

Journal: Acta crystallographica. Section E, Structure reports online20120101

Title: Studies on log Po/w of quinoxaline di-N-oxides: a comparison of RP-HPLC experimental and predictive approaches.

Journal: Molecules (Basel, Switzerland)20110913

Title: In silico quantitative structure-activity relationship studies on P-gp modulators of tetrahydroisoquinoline-ethyl-phenylamine series.

Journal: BMC structural biology20110101

Title: Synthesis and antimycobacterial activity of new quinoxaline-2-carboxamide 1,4-di-N-oxide derivatives.

Journal: European journal of medicinal chemistry20101001

Title: Structure-activity relationship (SAR) studies of quinoxalines as novel HCV NS5B RNA-dependent RNA polymerase inhibitors.

Journal: Bioorganic & medicinal chemistry letters20070315

Title: Synthesis and antimycobacterial activity of new quinoxaline-2-carboxamide 1,4-di-N-oxide derivatives.

Journal: Bioorganic & medicinal chemistry20030515

Title: Synthesis and antimycobacterial activity of pyrazine and quinoxaline derivatives.

Journal: Journal of medicinal chemistry20021205

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