3166-00-5

Usage

Uses

Used in Pharmaceutical Industry:
N-Amidinobenzamide is used as a building block for the preparation of various pharmaceutical compounds due to its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
N-Amidinobenzamide is used as a reagent in organic synthesis, facilitating the creation of complex organic molecules that can be utilized in a wide range of chemical and pharmaceutical processes.
Used in Anticancer Applications:
N-Amidinobenzamide is used as a potential anticancer agent, exhibiting biological activities that may contribute to the inhibition of cancer cell growth and the development of novel cancer treatments.
Used in Antiviral Applications:
N-Amidinobenzamide is used as a potential antiviral agent, showing promise in the development of treatments for viral infections by interfering with viral replication or other essential processes.
Used in Enzyme Inhibition Research:
N-Amidinobenzamide is used as an inhibitor of specific enzyme pathways, which may play a role in the development of certain diseases. Its potential use in this area is under investigation for the development of targeted therapies.

InChI:InChI=1/C8H9N3O/c9-8(10)11-7(12)6-4-2-1-3-5-6/h1-5H,(H4,9,10,11,12)

Upstream product

• 93-89-0 benzoic acid ethyl ester 
• 113-00-8 guanidine nitrate 
• 7788-14-9 5-phenyl-1,2,4-oxadiazol-3-amine 
• 614-23-3 N-benzoylthiourea 
• 98-88-4 benzoyl chloride 
• 74764-17-3 2-[(pyridin-2-yl)amino]ethylamine 
• 50-01-1 guanidine hydrochloride 

Downstream Products

• 29397-44-2 5,5'-diphenyl-3,3'-triazene-1,3-diyl-bis-[1,2,4]thiadiazole; sodium salt 
• 27182-74-7 bis-(2-nitro-phenylsulfanyl)-(5-phenyl-[1,2,4]thiadiazol-3-yl)-amine 
• 27182-70-3 4,4'-dinitro-N-(5-phenyl-[1,2,4]thiadiazol-3-yl)-dibenzamide 
• 27182-69-0 3,3'-dimethyl-N-(5-phenyl-[1,2,4]thiadiazol-3-yl)-dibenzamide 
• 27185-76-8 (5-phenyl-[1,2,4]thiadiazol-3-yl)-trityl-amine 
• 27182-73-6 S-(2-nitro-phenyl)-N-(5-phenyl-[1,2,4]thiadiazol-3-yl)-thiohydroxylamine 
• 27185-75-7 benzhydryl-(5-phenyl-[1,2,4]thiadiazol-3-yl)-amine 
• 27182-68-9 3-methyl-N-(5-phenyl-[1,2,4]thiadiazol-3-yl)-benzamide 
• 27182-54-3 5-phenyl-1,2,4-thiadiazol-3-amine 
• 7788-14-9 5-phenyl-1,2,4-oxadiazol-3-amine 
• 58287-41-5 3-benzoylamino-5-methyl-1,2,4-thiadiazole 
• 13365-12-3 5-phenyl-2-phenylsulfonylamino-1,3,4-oxadiazole 

Relevant academic research and scientific papers

Iodine-mediated multi-component reactions: Readily access to tetrazoles and guanidines

Environmentally benign syntheses of One-pot sequential reactions of benzoyl chloride with amines followed by the treatment of molecular I2 reagent under basic conditions provide benzoyl tetrazoles and guanidines in moderate to excellent yields. This one-pot synthesis has several advantages such as mild reaction conditions, short reaction time, convenient workup, high yields, using cheap and readily available reagent molecular Iodine. In addition, functional group tolerance has been explored.

Photoinduced molecular rearrangements. Some comments on the ring-photoisomerization of 1,2,4-oxadiazoles into 1,3,4-oxadiazoles

The ring-photoisomerization of 3-amino- and 3-methylamino-5-phenyl-1,2,4-oxadiazoles into the corresponding 2-amino- and 2-methylamino-5-phenyl-1,3,4-oxadiazoles has been reinvestigated by examining the effect of a base on the photoreaction. On irradiatin

IMIDAZOLYL ALKYL GUANIDINE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL PREPARATIONS CONTAINING THESE COMPOUNDS

New imidazolylalkyl-guanidine derivatives are described, which by virtue of their agonistic action on histamine-H 2 receptors and in part also due to their additional H 1-antagonistic receptor activity can be used in the treatment of cardiac diseases, certain forms of hypertension and diseases of arterial occlusion.These imidazolylalkyl-guanidine derivatives correspond to the general formula I: STR1