56108-05-5

Basic information

• Product Name: Benzenecarboximidic acid, 4-fluoro-, methyl ester, hydrochloride
• CAS NO: 56108-05-5
• Molecular Formula: C8H8FNO.ClH
• Molecular Weight: 189.617
• Mol File: 56108-05-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenecarboximidic acid, 4-fluoro-, methyl ester, hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarboximidic acid, 4-fluoro-, methyl ester, hydrochloride(56108-05-5)
• EPA Substance Registry System: Benzenecarboximidic acid, 4-fluoro-, methyl ester, hydrochloride(56108-05-5)

Safety Data

• Hazardous Substances Data: 56108-05-5(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 1194-02-1 4-fluorobenzonitrile 

Downstream Products

• 1255777-13-9 2-(3-(4-fluorophenyl)-1H-1,2,4-triazol-5-yl)acetonitrile 
• 1314887-65-4 2-(3-(4-fluorophenyl)-1H-1,2,4-triazol-5-yl)ethanamine 
• 1314887-47-2 3-(2-(4-fluorophenyl)oxazol-4-yl)-3-hydroxypropanenitrile 
• 1314887-46-1 1-(2-(4-fluorophenyl)oxazol-4-yl)ethanone 
• 1314887-38-1 2-amino-1-(2-(4-fluorophenyl)oxazol-4-yl)ethanol 
• 1314887-37-0 2-(2-(4-fluorophenyl)oxazol-4-yl)-2-hydroxyacetonitrile 
• 152940-51-7 2-(4-fluorophenyl)oxazole-4-carbaldehyde 
• 1065102-64-8 methyl 2-(4-fluorophenyl)-1,3-oxazole-4-carboxylate 
• 885273-80-3 (2-(4-fluorophenyl)oxazol-4-yl)methanol 
• 1314419-49-2 methyl 2-(4-fluorophenyl)-4,5-dihydrooxazole-4-carboxylate 
• 1379505-91-5 C₁₅H₁₄FNO₃S 
• 1379505-99-3 C₂₅H₂₈FNO₂SSi 
• 456-14-4 4-fluorobenzamidine hydrochloride 
• 133118-45-3 2-<2-(4-fluorophenyl)-4-imidazolyl>ethanamine 

Relevant articles and documents

NOVEL OXABOROLE ANALOGS AND USES THEREOF

This application describes compounds, compositions, and methods which are useful in treating, preventing, inhibiting, ameliorating, or eradicating the pathology and/or symptomology of a disease caused by a parasite.

Efficient synthesis of α-tertiary α-silylamines from aryl sulfonylimidates via one-pot, sequential C-Si/C-C bond formations

An efficient and flexible route for the synthesis of α-tertiary (α,α-dibranched) α-silylamines via sequential reactions of sulfonylimidates using readily available phenyldimethylsilyllithium and Grignard reagents is described. The procedure allows successive formation of C-Si/C-C bonds in a single flask.

Histamine analogues. 33rd communication: 2-phenylhistamines with high histamine H1-agonistic activity

2-Phenylhistamines with various substituents at the phenyl ring were synthesized and the influence of substitution in ortho, meta or para position on histamine H1-agonistic activity was investigated.Compounds with high activity occured in the meta phenyl series.Increased activity in the guinea-pig ileum assay was achieved by monosubstitution with halogen on the phenyl ring. 2-ethanamine (12) is the most potent highly selective H1-agonist known so far, showing 87percent relative potency compared with histamine and full efficacy at theH1-receptor.Relative activities of the 3-chloro analogue (11) and the 3-methyl analogue (13) are 81percent and 29percent, respectively.Histamine H2-activity could not be detected. 2-Phenylhistamines are available via reaction of the corresponding benzimidates with 2-oxo-4-phthalimido-1-butyl acetate (6) in liquid ammonia.