89410-18-4

Basic information

• Product Name: BENZENE, 1-CYCLOPENTYL-4-NITRO-
• Synonyms: BENZENE, 1-CYCLOPENTYL-4-NITRO-;1-cyclopentyl-4-nitrobenzene
• CAS NO: 89410-18-4
• Molecular Formula: C₁₁H₁₃NO₂
• Molecular Weight: 191.23
• Mol File: 89410-18-4.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BENZENE, 1-CYCLOPENTYL-4-NITRO-(CAS DataBase Reference)
• NIST Chemistry Reference: BENZENE, 1-CYCLOPENTYL-4-NITRO-(89410-18-4)
• EPA Substance Registry System: BENZENE, 1-CYCLOPENTYL-4-NITRO-(89410-18-4)

Safety Data

• Hazardous Substances Data: 89410-18-4(Hazardous Substances Data)

Upstream product

• 1040745-70-7 cyclopentyltrifluoro-λ⁴-borane potassium salt 
• 100-00-5 4-chlorobenzonitrile 
• 586-78-7 para-nitrophenyl bromide 
• 700-88-9 cyclopentylbenzene 
• 71-43-2 benzene 
• 142-29-0 cyclopentene 
• 100-25-4 para-dinitrobenzene 
• 49623-12-3 9-cyclopentyl-9-bora-bicyclo[3.3.1]nonane 

Downstream Products

• 1449476-28-1 N-(4-cyclopentyl-2-nitrophenyl)acetamide 
• 1449475-73-3 4-cyclopentylbenzene-1,2-diamine 
• 67330-66-9 2-cyclopentyl-aniline 
• 20029-53-2 (4-aminophenyl)cyclopentane 

Relevant articles and documents

BENZIIMIDAZOLE AND IMIDAZOPYRIDINE DERIVATIVES AS SODIUM CHANNEL MODULATORS

The invention relates to benzimidazole and imidazopyridine derivatives, to their use in medicine, to compositions containing them, to processes for their preparation and to intermediates used in such processes. More particularly the invention relates to new Nav1.8 modulators of formula (I) or pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, R7. X and Y are as defined in the description. Nav1.8 modulators are potentially useful in the treatment of a wide range of disorders, particularly pain.

Efficient cross-coupling of secondary alkyltrifluoroborates with aryl chlorides-reaction discovery using parallel microscale experimentation

Microscale parallel experimentation was used to discover three catalyst systems capable of coupling secondary organotrifluoroborates with sterically and electronically demanding aryl chlorides and bromides. The ensuing results represent the first comprehensive study of alkylboron coupling to aryl chlorides and, in particular, using secondary alkylboron partners. A ligand-dependent β-hydride elimination/reinsertion mechanism was implicated in the cross-coupling of more hindered substrates, leading to isomeric mixtures of coupled products in some cases. Copyright

Methods and compositions for treating pain

The present application relates to compounds and methods for treating pain, incontinence and other conditions.