34649-19-9

Usage

InChI:InChI=1/C5H2Br2N2/c6-4-1-3(2-8)9-5(4)7/h1,9H

Upstream product

• 4513-94-4 1H-pyrrole-2-carbonitrile 
• 51148-00-6 4,5-dibromo-1H-pyrrole-2-carbaldehyde oxime 

Downstream Products

• 1402652-60-1 7-(4-methoxyphenyl)-2,3-dihydro-1H-pyrrolizine-5-carbonitrile 
• 1402652-61-2 6-bromo-7-(4-methoxyphenyl)-2,3-dihydro-1H-pyrrolizine-5-carbonitrile 
• 1402652-62-3 C₁₄H₁₁BrN₂O 
• 1402652-63-4 methyl 4-(5-cyano-7-(4-hydroxyphenyl)-2,3-dihydro-1H-pyrrolizin-6-yl)-3,5-dimethylfuran-2-carboxylate 
• 1402652-64-5 4-(5-cyano-7-(4-hydroxyphenyl)-2,3-dihydro-1H-pyrrolizin-6-yl)-3,5-dimethylfuran-2-carboxylic acid 
• 1402652-65-6 6-(2,4-dimethylfuran-3-yl)-7-(4-hydroxyphenyl)-2,3-dihydro-1H-pyrrolizine-5-carbonitrile 
• 1402652-23-6 6-(2,4-dimethylfuran-3-yl)-N'-hydroxy-7-(4-hydroxyphenyl)-2,3-dihydro-1H-pyrrolizine-5-carboximidamide 
• 1402652-58-7 1-allyl-4-(4-methoxyphenyl)-5-vinyl-1H-pyrrole-2-carbonitrile 
• 1402652-59-8 7-(4-methoxyphenyl)-3H-pyrrolizine-5-carbonitrile 
• 1346162-56-8 (2'S)-4,5-dibromo-1-[1'-(tert-butyldiphenylsilyloxy)-4'-hydroxybutan-2'-yl]-1H-pyrrole-2-carbonitrile 
• 1346162-54-6 (2'S)-4,5-dibromo-1-(1'-benzoyloxy-4'-hydroxybutan-2'-yl)-1H-pyrrole-2-carbonitrile 
• 1346162-68-2 (2'S)-4,5-dibromo-1-[4'-methoxy-1'-(p-toluenesulfonyloxy)butan-2'-yl]-1H-pyrrole-2-carbonitrile 
• 1346162-66-0 (2'S)-4,5-dibromo-1-[1'-(tert-butyldiphenylsilyloxy)-4'-methoxybutan-2'-yl]-1H-pyrrole-2-carbonitrile 

Relevant academic research and scientific papers

FUSED PYRROLE DERIVATES AS ESTROGEN RECEPTOR LIGANDS

The invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein Z, A, B, D,E, G, M1, M2, M3, M4, M5, M6, p, q, r, R3, R4, R5 and R6 are as defined in the specification. The invention also provides the use of such co

Phosphonium salt-catalysed synthesis of nitriles from in situ activated oximes

A metal-free catalytic method for the conversion of aromatic and aliphatic aldoximes to nitriles at room temperature using oxalyl chloride (1.2 equiv) in combination with 5 mol % of triphenylphosphine oxide is reported. Of the many potential pathways leading from oxime to nitrile a manifold involving chlorophosphonium salt-catalysed decomposition of oxime chlorooxalates formed in situ is shown to be operative.

Antimicrobial and plant-active 4,5-dihalopyrrole-2-carbonitriles

Phytoresponsive and antimicrobial compositions containing, as the active ingredient, a 4,5-dihalopyrrole-2-carbonitrile and methods of combatting microorganisms and plant growth comprising applying an effective antimicrobial or phytotoxic quantity of the active ingredient to a surface to be disinfected or to undesirable plant growth.