56406-50-9

Basic information

• Product Name: 3-NITROBENZAMIDINE HYDROCHLORIDE
• Synonyms: 3-nitrobenzenecarboximidamidemonohydrochloride;3-nitro-benzenecarboximidamidmonohydrochloride;m-nitrobenzamidinehydrochloride;m-nitro-benzamidinhydrochloride;3-NITROBENZAMIDINE HYDROCHLORIDE;3-nitrobenzamidinium hydrochloride;Benzamidine, m-nitro, hydrochloride.;3-Nitrobenzamidine hydrochloride,97%
• CAS NO: 56406-50-9
• Molecular Formula: C₇H₇N₃O₂*ClH
• Molecular Weight: 201.61
• EINECS: 260-159-9
• Product Categories: Imines/Amidines;Nitrogen Compounds;Organic Building Blocks
• Mol File: 56406-50-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: 245-248 °C(lit.)
• Boiling Point: 301.7°C at 760 mmHg
• Flash Point: 136.3°C
• Appearance: Light yellow microcrystalline powder
• Vapor Pressure: 0.00103mmHg at 25°C
• CAS DataBase Reference: 3-NITROBENZAMIDINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-NITROBENZAMIDINE HYDROCHLORIDE(56406-50-9)
• EPA Substance Registry System: 3-NITROBENZAMIDINE HYDROCHLORIDE(56406-50-9)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• RTECS: CV6295000
• Hazardous Substances Data: 56406-50-9(Hazardous Substances Data)

Usage

Chemical Properties

Light yellow microcrystalline powder

Uses

3-Nitrobenzamidine hydrochloride was used as reagent during the synthesis of (Z)-3-benzoylamino-4-dimethylamino-2-oxo-3-butene.

InChI:InChI=1/C7H7N3O2/c8-7(9)5-2-1-3-6(4-5)10(11)12/h1-4H,(H3,8,9)/p+1

Upstream product

• 57508-53-9 3-nitrobenzenecarboximidic acid ethyl ester monohydrochloride 
• 619-24-9 3-nitrobenzonitrile 

Downstream Products

• 77139-57-2 5-chloro-2-m-nitrophenylpyrimidine 
• 3459-66-3 3-aminobenzamidine 
• 3459-67-4 3-aminobenzamidine dihydrochloride 
• 619-24-9 3-nitrobenzonitrile 
• 1449522-80-8 5-methyl-2-(3-nitrophenyl)-4-phenyl-1H-imidazole 
• 1449522-81-9 4-(4-methoxyphenyl)-5-methyl-2-(3-nitrophenyl)-1H-imidazole 
• 56406-34-9 2-(3-nitro-phenyl)-6-oxo-1,6-dihydro-pyrimidine-5-carboxylic acid 
• 477879-51-9 N-{1-[3-(3-nitrophenyl)-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl]propyl}acetamide 
• 873663-34-4 6-hydroxy-2-(3-nitrophenyl)pyrimidin-4(3H)-one 
• 90110-85-3 5-hydrazino-3-(3-nitro-phenyl)-[1,2,4]thiadiazole 
• 107664-91-5 4-(4-diethylamino-phenylimino)-5-heptadecyl-2-[3-(3-nitro-phenyl)-[1,2,4]thiadiazol-5-yl]-2,4-dihydro-pyrazol-3-one 
• 98544-27-5 5-heptadecyl-2-[3-(3-nitro-phenyl)-[1,2,4]thiadiazol-5-yl]-1,2-dihydro-pyrazol-3-one 
• 95942-60-2 4-(4-diethylamino-phenylimino)-5-methyl-2-[3-(3-nitro-phenyl)-[1,2,4]thiadiazol-5-yl]-2,4-dihydro-pyrazol-3-one 
• 95559-67-4 4-(4-dimethylamino-phenylimino)-5-methyl-2-[3-(3-nitro-phenyl)-[1,2,4]thiadiazol-5-yl]-2,4-dihydro-pyrazol-3-one 

Relevant articles and documents

Synthesis and structure of aroylamidines and N-arylbenzamidines hydrochlorides

Aroylamidines can be obtained as salts in a reaction of the corresponding arylcarbonitriles with anhydrous ethanol in the presence of dry HCl followed by treating intermediate imidoesters with alcoholic solution of ammonia. N-Arylbenzamidines are obtained by reacting benzonitrile with arylamines in the presence of AlCl3. The structure of arylamines and the reaction conditions signifi cantly affect the yield of the target product, and sometimes the very possibility of its preparation. Pleiades Publishing, Ltd., 2012.

Novel heterocycles 3

The invention relates to 7-(4-tert butyl-cyclohexyl)-imidazotriazinones, processes for their preparation and their use in medicaments, esp. for the treatment and/or prophylaxis of inflammatory processes and/or immune diseases.