CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE
CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE
CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE
CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE
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  • CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE
  • CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE
  • CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE
  • CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE

CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE

Name: 6-BROMO-5-AZAINDOLE CAS No.1000342-71-1 MF: C7H5BrN2 MW: 197.03 Purity:97% Package: 5g,25g,100g,500g,1kg,25kg Worldwide Delivery

Categories:

Analytical Chemicals

Product introduction

Introduction and application of CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE

Pyrroloquinoline quinones are a class of naturally occurring bioactive natural products that have been isolated from plants and fungi. Pyrroloquinoline quinone is an important intermediate in the synthesis of many other biologically active natural products. The pyrrole ring is synthesized by two different methods: (1) the oxidation of 2-pyridone, or (2) the reaction of methyl 4-hydroxypyrimidine-2-carboxylate with methylamine. Synthesis can be accomplished through a number of synthetic strategies, including bioorganic chemistry, organic chemistry, and synthetic strategies. 

Synonyms:

6-bromo-1H-pyrrolo[3,2-c]pyridine;

 

Specification of CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE

 

ITEMS

SPECIFICATION

CAS No.

1000342-71-1

MF

C7H5BrN2

MW

197.03

Boiling point

362.0±22.0 °C(Predicted)

Density(25℃,g/cm3)

1.770

acidity coefficient(pKa)

14.27±0.40(Predicted)

Package of CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE

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

Transportation: by courier/ by air/ by sea

Related Articles of CAS No.1000342-71-1 | 6-BROMO-5-AZAINDOLE

 

Recent developments in the synthesis of azaindoles from pyridine and pyrrole building blocks

DR Motati, R Amaradhi, T Ganesh - Organic Chemistry Frontiers, 2021 - pubs.rsc.org

… The reaction of appropriately substituted 4-amino-2-bromo-5-iodopyridine 17a and
heteroaromatic alkyne and further functional group transformations produced 6-bromo-5-azaindole …

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