274-95-3,MFCD06245377
Catalog No.:AA003QWT

274-95-3 | Imidazo[1,2-a]pyrimidine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$11.00   $8.00
- +
1g
97%
in stock  
$32.00   $23.00
- +
5g
97%
in stock  
$52.00   $37.00
- +
10g
97%
in stock  
$102.00   $72.00
- +
100g
97%
in stock  
$879.00   $615.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003QWT
Chemical Name:
Imidazo[1,2-a]pyrimidine
CAS Number:
274-95-3
Molecular Formula:
C6H5N3
Molecular Weight:
119.1240
MDL Number:
MFCD06245377
SMILES:
c1ccn2c(n1)ncc2
Properties
Properties
 
Form:
Solid  
MP:
129-130°C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
105  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.1  

Synonyms
 
  
Literature

Title: Generation and exploration of new classes of antitubercular agents: The optimization of oxazolines, oxazoles, thiazolines, thiazoles to imidazo[1,2-a]pyridines and isomeric 5,6-fused scaffolds.

Journal: Bioorganic & medicinal chemistry 20120401

Title: Lifelong CRF overproduction is associated with altered gene expression and sensitivity of discrete GABA(A) and mGlu receptor subtypes.

Journal: Psychopharmacology 20120201

Title: Systematic structure modifications of imidazo[1,2-a]pyrimidine to reduce metabolism mediated by aldehyde oxidase (AO).

Journal: Journal of medicinal chemistry 20111110

Title: Structure-activity relationship of 4(5)-aryl-2-amino-1H-imidazoles, N1-substituted 2-aminoimidazoles and imidazo[1,2-a]pyrimidinium salts as inhibitors of biofilm formation by Salmonella typhimurium and Pseudomonas aeruginosa.

Journal: Journal of medicinal chemistry 20110127

Title: Post Groebke-Blackburn multicomponent protocol: synthesis of new polyfunctional imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrimidine derivatives as potential antimicrobial agents.

Journal: European journal of medicinal chemistry 20101201

Title: 5-HT1A receptor blockade reverses GABA(A) receptor alpha3 subunit-mediated anxiolytic effects on stress-induced hyperthermia.

Journal: Psychopharmacology 20100801

Title: Efficient one-pot, two-step, microwave-assisted procedure for the synthesis of polysubstituted 2-aminoimidazoles.

Journal: Organic letters 20061207

Title: 8-Fluoroimidazo[1,2-a]pyridine: synthesis, physicochemical properties and evaluation as a bioisosteric replacement for imidazo[1,2-a]pyrimidine in an allosteric modulator ligand of the GABA A receptor.

Journal: Bioorganic & medicinal chemistry letters 20060315

Title: Palladium-catalyzed regioselective arylation of imidazo[1,2-a]pyrimidine.

Journal: Organic letters 20031211

Title: Effect of imidazo[1,2-a]pyrimidine derivatives on leukocyte function.

Journal: Inflammation research : official journal of the European Histamine Research Society ... [et al.] 20010601

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SDS
Tags:274-95-3 Molecular Formula|274-95-3 MDL|274-95-3 SMILES|274-95-3 Imidazo[1,2-a]pyrimidine
Catalog No.: AA003QWT
274-95-3,MFCD06245377
274-95-3 | Imidazo[1,2-a]pyrimidine
Pack Size: 250mg
Purity: 97%
in stock
$11.00 $8.00
Pack Size: 1g
Purity: 97%
in stock
$32.00 $23.00
Pack Size: 5g
Purity: 97%
in stock
$52.00 $37.00
Pack Size: 10g
Purity: 97%
in stock
$102.00 $72.00
Pack Size: 100g
Purity: 97%
in stock
$879.00 $615.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003QWT
Chemical Name: Imidazo[1,2-a]pyrimidine
CAS Number: 274-95-3
Molecular Formula: C6H5N3
Molecular Weight: 119.1240
MDL Number: MFCD06245377
SMILES: c1ccn2c(n1)ncc2
Properties
Form: Solid  
MP: 129-130°C  
Storage: Keep in dry area;Room Temperature;  
Complexity: 105  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.1  
62:   
Literature fold

Title: Generation and exploration of new classes of antitubercular agents: The optimization of oxazolines, oxazoles, thiazolines, thiazoles to imidazo[1,2-a]pyridines and isomeric 5,6-fused scaffolds.

Journal: Bioorganic & medicinal chemistry20120401

Title: Lifelong CRF overproduction is associated with altered gene expression and sensitivity of discrete GABA(A) and mGlu receptor subtypes.

Journal: Psychopharmacology20120201

Title: Systematic structure modifications of imidazo[1,2-a]pyrimidine to reduce metabolism mediated by aldehyde oxidase (AO).

Journal: Journal of medicinal chemistry20111110

Title: Structure-activity relationship of 4(5)-aryl-2-amino-1H-imidazoles, N1-substituted 2-aminoimidazoles and imidazo[1,2-a]pyrimidinium salts as inhibitors of biofilm formation by Salmonella typhimurium and Pseudomonas aeruginosa.

Journal: Journal of medicinal chemistry20110127

Title: Post Groebke-Blackburn multicomponent protocol: synthesis of new polyfunctional imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrimidine derivatives as potential antimicrobial agents.

Journal: European journal of medicinal chemistry20101201

Title: 5-HT1A receptor blockade reverses GABA(A) receptor alpha3 subunit-mediated anxiolytic effects on stress-induced hyperthermia.

Journal: Psychopharmacology20100801

Title: Efficient one-pot, two-step, microwave-assisted procedure for the synthesis of polysubstituted 2-aminoimidazoles.

Journal: Organic letters20061207

Title: 8-Fluoroimidazo[1,2-a]pyridine: synthesis, physicochemical properties and evaluation as a bioisosteric replacement for imidazo[1,2-a]pyrimidine in an allosteric modulator ligand of the GABA A receptor.

Journal: Bioorganic & medicinal chemistry letters20060315

Title: Palladium-catalyzed regioselective arylation of imidazo[1,2-a]pyrimidine.

Journal: Organic letters20031211

Title: Effect of imidazo[1,2-a]pyrimidine derivatives on leukocyte function.

Journal: Inflammation research : official journal of the European Histamine Research Society ... [et al.]20010601

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