55-22-1,MFCD00006429
Catalog No.:AA0034Z4

55-22-1 | isonicotinic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$12.00   $8.00
- +
10g
98%
in stock  
$13.00   $9.00
- +
25g
98%
in stock  
$18.00   $12.00
- +
100g
98%
in stock  
$28.00   $19.00
- +
250g
98%
in stock  
$63.00   $44.00
- +
500g
98%
in stock  
$73.00   $51.00
- +
  • Technical Information
  • Properties
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0034Z4
Chemical Name:
isonicotinic acid
CAS Number:
55-22-1
Molecular Formula:
C6H5NO2
Molecular Weight:
123.1094
MDL Number:
MFCD00006429
SMILES:
OC(=O)c1ccncc1
Properties
Properties
 
BP:
396°C at 760 mmHg  
Form:
Solid  
MP:
≥300 °C(lit.)  
Refractive Index:
1.5423 (estimate)  
Solubility:
6g/l  
Storage:
Keep in dry area;Room Temperature;  


Literature

Title: Seng KY, et al. Population pharmacokinetic analysis of isoniazid, acetylisoniazid, and isonicotinic acid in healthy volunteers. Antimicrob Agents Chemother. 2015 Nov;59(11):6791-9.

Application
Isonicotinic acid (IN) emerges as a versatile compound with a wide range of applications in organic synthesis and coordination chemistry. Its significance is evident in its role as an organocatalyst in one-pot four-component condensation reactions, facilitating the synthesis of pyranopyrazoles and other heterocyclic compounds with diverse structural motifs and potential biological activities. Additionally, Isonicotinic acid serves as an organic ligand in the preparation of copper(I) halide coordination polymers, such as [CuBr(IN)]n, utilizing hydrothermal methods, offering opportunities for the design and synthesis of novel coordination polymers with tailored properties. Furthermore, it serves as a crucial starting material for the synthesis of cation-dimers exhibiting potent antimalarial activity, highlighting its importance in drug discovery and medicinal chemistry. With its diverse applications in synthetic chemistry and coordination chemistry, Isonicotinic acid emerges as a valuable tool for the development of functional materials and biologically active compounds.
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Tags:55-22-1 Molecular Formula|55-22-1 MDL|55-22-1 SMILES|55-22-1 isonicotinic acid
Catalog No.: AA0034Z4
55-22-1,MFCD00006429
55-22-1 | isonicotinic acid
Pack Size: 1g
Purity: 98%
in stock
$12.00 $8.00
Pack Size: 10g
Purity: 98%
in stock
$13.00 $9.00
Pack Size: 25g
Purity: 98%
in stock
$18.00 $12.00
Pack Size: 100g
Purity: 98%
in stock
$28.00 $19.00
Pack Size: 250g
Purity: 98%
in stock
$63.00 $44.00
Pack Size: 500g
Purity: 98%
in stock
$73.00 $51.00
Quantity
- +
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Technical Information
Catalog Number: AA0034Z4
Chemical Name: isonicotinic acid
CAS Number: 55-22-1
Molecular Formula: C6H5NO2
Molecular Weight: 123.1094
MDL Number: MFCD00006429
SMILES: OC(=O)c1ccncc1
Properties
BP: 396°C at 760 mmHg  
Form: Solid  
MP: ≥300 °C(lit.)  
Refractive Index: 1.5423 (estimate)  
Solubility: 6g/l  
Storage: Keep in dry area;Room Temperature;  
Application fold
Isonicotinic acid (IN) emerges as a versatile compound with a wide range of applications in organic synthesis and coordination chemistry. Its significance is evident in its role as an organocatalyst in one-pot four-component condensation reactions, facilitating the synthesis of pyranopyrazoles and other heterocyclic compounds with diverse structural motifs and potential biological activities. Additionally, Isonicotinic acid serves as an organic ligand in the preparation of copper(I) halide coordination polymers, such as [CuBr(IN)]n, utilizing hydrothermal methods, offering opportunities for the design and synthesis of novel coordination polymers with tailored properties. Furthermore, it serves as a crucial starting material for the synthesis of cation-dimers exhibiting potent antimalarial activity, highlighting its importance in drug discovery and medicinal chemistry. With its diverse applications in synthetic chemistry and coordination chemistry, Isonicotinic acid emerges as a valuable tool for the development of functional materials and biologically active compounds.
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