![6-Bromo-1H-pyrrolo[3,2-C]pyridine](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F281803-6-bromo-1h-pyrrolo-32-c-pyridine.webp&w=3840&q=75)
CAS 1000342-71-1: 6-Bromo-1H-pyrrolo[3,2-C]pyridine
Formula:C7H5BrN2
InChI:InChI=1S/C7H5BrN2/c8-7-3-6-5(4-10-7)1-2-9-6/h1-4,9H
InChI key:InChIKey=IRXFHLHFJHIJTO-UHFFFAOYSA-N
SMILES:BrC=1C=C2C(=CN1)C=CN2
Synonyms:- 1H-Pyrrolo[3,2-C]pyridine, 6-bromo-
- 6-Bromo-5-azaindole
- 6-Bromo-1H-pyrrolo[3,2-c]pyridine
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Found 4 products.
1H-Pyrrolo[3,2-c]pyridine, 6-bromo-
CAS:Formula:C7H5BrN2Purity:98%Color and Shape:SolidMolecular weight:197.0326-Bromo-1H-pyrrolo[3,2-c]pyridine
CAS: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. The mechanisms for each step in the synthesis are discussed in detail below.Formula:C7H5BrN2Purity:Min. 95%Color and Shape:SolidMolecular weight:197.03 g/mol6-Bromo-1H-pyrrolo[3,2-c]pyridine
CAS:6-Bromo-1H-pyrrolo[3,2-c]pyridineFormula:C7H5BrN2Purity:99%Color and Shape: white powderMolecular weight:197.03g/mol6-Bromo-1H-pyrrolo[3,2-c]pyridine
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:197.03500366210938