CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole
CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole
CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole
CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole
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  • CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole
  • CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole
  • CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole
  • CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole

CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole

Name: 4-Iodo-1-methyl-1H-imidazole CAS No.71759-87-0 MF: C4H5IN2 MW: 208 Purity:97% Package: 5g,25g,100g,500g,1kg,25kg Worldwide Delivery

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Analytical Chemicals

Product introduction

Introduction and application of CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole

4-Iodo-1-methyl-1H-imidazole is a trifluoroethylamine that inhibits the activity of tyrosine kinases. It binds to the active site of tyrosine kinase and prevents the binding of ATP, preventing phosphorylation and activation of downstream substrates. 4-Iodo-1-methyl-1H-imidazole has been shown to inhibit the proliferation of tumor xenografts in mice, as well as inhibiting headgroup binding and cellular proliferation in vitro. This agent also has a nanomolar range and high selectivity for protein kinases, which may make it suitable for therapeutic purposes.

 

Specification of CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole

 

CAS No.

71759-87-0

MF

C4H5IN2

MW

208

Melting point

51-54°C

Boiling point

299.0±13.0 °C(Predicted)

Density(25℃,g/cm3)

2.07±0.1 g/cm3(Predicted)

acidity coefficient(pKa)

4.46±0.61(Predicted)

Package of CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole

Package:100g; 500g; 1kg; 25kg;bulk package

Transportation: by courier/ by air/ by sea

Related Articles of CAS No.71759-87-0 | 4-Iodo-1-methyl-1H-imidazole

[PDF] Synthesis of imidazole core based small molecules for the treatment of SMA

S Barranco Campos - 2019 - bora.uib.no

… Both 4-bromo-1-methyl-1H-imidazole 22 and 4-iodo-1-methyl-1H-imidazole 23 were
synthesized by following one of the procedures attempted for the synthesis of 17. The …

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