5005-14-1

Basic information

• Product Name: Benzamide, N-2-benzothiazolyl-
• CAS NO: 5005-14-1
• Molecular Formula: C14H10N2OS
• Molecular Weight: 254.312
• Mol File: 5005-14-1.mol
• Article Data: 37

Chemical Properties

• CAS DataBase Reference: Benzamide, N-2-benzothiazolyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-2-benzothiazolyl-(5005-14-1)
• EPA Substance Registry System: Benzamide, N-2-benzothiazolyl-(5005-14-1)

Safety Data

• Hazardous Substances Data: 5005-14-1(Hazardous Substances Data)

Upstream product

• 136-95-8 2-amino-benzthiazole 
• 98-88-4 benzoyl chloride 
• 133494-00-5 1-Benzoyl-3-(2-mercapto-phenyl)-thiourea 
• 137-07-5 2-amino-benzenethiol 
• 532-55-8 Benzoyl isothiocyanate 
• 1141-88-4 2-Aminophenyl disulfide 
• 1126640-07-0 2-phenyl-3-(N-t-butyl)-amino-benzo[d]imidazo[2,1-b]thiazole 
• 1934-92-5 N-methyl-N-phenyl-benzamide 
• 15150-25-1 N-cyanobenzamide 
• 5391-29-7 N-(2-bromophenyl)-N'-benzoylthiourea 
• 1006863-65-5 N-(2-iodophenyl)-N'-benzoylthiourea 
• 21406-30-4 N-Benzoylamino-dithiokohlensaeuremethylester 
• 848417-68-5 3,6-dibenzoyloxy-1,2-pyridazine 
• 24786-18-3 dimethyl N-benzoyldithiocarbonimidate 

Downstream Products

• 51579-08-9 2-phenyl-s-triazolo<5,1-b>-benzothiazole 
• 136-95-8 2-amino-benzthiazole 
• 127801-98-3 ethyl 2-[2-(benzoylimino)benzo[d]thiazol-3(2H)-yl]acetate 
• 1428621-28-6 2-[2-(benzoylimino)benzo[d]thiazol-3(2H)-yl]acetic acid 
• 91506-73-9 1-(2'-benzothiazolyl)-5-phenyltetrazole 
• 118215-06-8 N-(benzothiazol-2-yl)benzothioamide 
• 7267-74-5 N-(3-methyl-3H-benzothiazol-2-ylidene)-benzamide 
• 51578-96-2 3-amino-2-benzoylamino-benzothiazolium; 2,4,6-trimethyl-benzenesulfonate 

Relevant articles and documents

Synthesis and Structural Characterization of Palladium(II) Mixed-Ligand Complexes of N-(Benzothiazol-2-yl)benzamide and 1,2-Bis(diphenylphosphino)ethane

Three novel palladium(II) mixed-ligand complexes of N-(benzothiazol-2-yl)benzamide (HL) and 1,2-bis(diphenylphosphino)ethane (dppe), [Pd(HL)(dppe)]Cl2 (1), [Pd(L)(dppe)]Cl (2), and [Pd(L)2(dppe)] (3), were synthesized and fully chara

Metal-free oxidative decarbonylative halogenation of fused imidazoles

An efficient strategy has been developed for the deformylative halogenation of carbaldehyde imidazo-fused heterocycles in the presence of TBHP controlled by temperature. A convenient and sequential functionalization (C8 to C3) portrays the synthetic utility of the current method.N-Heterocycle benzamide products were also observedviathe ring opening of imidazopyridines through the cleavage of C-C bond at high temperatures. Features of this method include temperature-controlled excellent regioselectivity, mild conditions and functional group tolerance.

Sodium pyruvate as a peroxide scavenger in aerobic oxidation under carbene catalysis

NHC-Catalyzed aerobic oxidative reactions of imines and aldehydes have been developed by using sodium pyruvate as a novel and efficient peroxide scavenger. A structurally diverse set of imidates and amidines has been prepared from imines using this strategy. This general and efficient strategy features the use of sodium pyruvate as a novel and efficient peroxide scavenger and ambient air as the sole oxidant to efficiently control the NHC-catalyzed aerobic reaction pathway (selective realization of the oxidative pathway) under mild and green conditions. This journal is