127152-56-1

Basic information

• Product Name: (Benzothiazol-2-ylsulfanyl)-acetic acid [1-(4-chloro-phenyl)-meth-(E)-ylidene]-hydrazide
• Synonyms: (Benzothiazol-2-ylsulfanyl)-acetic acid [1-(4-chloro-phenyl)-meth-(E)-ylidene]-hydrazide
• CAS NO: 127152-56-1
• Molecular Weight: 361.876
• Mol File: 127152-56-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (Benzothiazol-2-ylsulfanyl)-acetic acid [1-(4-chloro-phenyl)-meth-(E)-ylidene]-hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: (Benzothiazol-2-ylsulfanyl)-acetic acid [1-(4-chloro-phenyl)-meth-(E)-ylidene]-hydrazide(127152-56-1)
• EPA Substance Registry System: (Benzothiazol-2-ylsulfanyl)-acetic acid [1-(4-chloro-phenyl)-meth-(E)-ylidene]-hydrazide(127152-56-1)

Safety Data

• Hazardous Substances Data: 127152-56-1(Hazardous Substances Data)

Upstream product

• 149-30-4 2-Mercaptobenzothiazole 
• 24044-88-0 ethyl 2-(benzo[d]thiazol-2-ylthio)acetate 
• 104-88-1 4-chlorobenzaldehyde 
• 24044-91-5 [(1,3-benzothiazol-2-ylthio)acetyl]hydrazine 

Downstream Products

• 144169-04-0 C₁₈H₁₄ClN₃O₂S₃ 
• 1311399-64-0 C₂₅H₁₈ClN₃O₂S₃ 

Relevant articles and documents

Synthesis of 2-mercapto benzothiazoles using LiBr as a catalyst

An efficient, fast and eco-friendly method for synthesis of some derivatives of 2-mercaptobenzothiazole under MW induced solvent free condition has been reported. LiBr acts as a catalyst for the condensation reactions. The structures of all the synthesize

Hydrazones of [(2-benzothiazolylthio)acetyl]hydrazine: Synthesis and antimicrobial activity

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