827-72-5

Basic information

• Product Name: 4-chloro-benzimidic acid ethyl ester
• Synonyms: 4-CHLORO-BENZIMIDIC ACID ETHYL ESTER;ethyl 4-chlorobenzimidate
• CAS NO: 827-72-5
• Molecular Formula: C₉H₁₀ClNO
• Molecular Weight: 183.63
• Mol File: 827-72-5.mol
• Article Data: 23

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-chloro-benzimidic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-benzimidic acid ethyl ester(827-72-5)
• EPA Substance Registry System: 4-chloro-benzimidic acid ethyl ester(827-72-5)

Safety Data

• Hazardous Substances Data: 827-72-5(Hazardous Substances Data)

Upstream product

• 623-03-0 4-Cyanochlorobenzene 
• 64-17-5 ethanol 
• 368-39-8 triethyloxonium fluoroborate 
• 619-56-7 4-chlorobenzamide 
• 17950-40-2 triethyloxonium hexaflourophosphate 
• 40546-41-6 ethyl-4-chlorobenzimidate hydrochloride 

Downstream Products

• 51234-85-6 dl-2-(p-chlorophenyl)-5-benzoxazolylacetic acid 
• 92666-88-1 2-[2-(4-Chloro-benzoyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinolin-1-yl]-acetamide 
• 106690-55-5 2-(4-chlorophenyl)-3H-pyrimidin-4-one 
• 132287-25-3 3-p-Chlorophenyl-5c-phenyl-2-oxa-4-aza-1r,6c-bicyclo<4.3.0>non-3-ene 
• 132287-26-4 3-p-Chlorophenyl-5c-phenyl-2-oxa-4-aza-1r,6c-bicyclo<4.4.0>dec-3-ene 
• 87768-87-4 2-(4-Chlorophenyl)-5,8-methano-r-4a,t-5,6,7,t-8,c-8a-hexahydro-4H-3,1-benzoxazine 
• 87768-87-4 (1S,2R,7S,8R)-4-(4-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7]undec-3-ene 
• 87768-84-1 2-(4-Chlorophenyl)-5,8-methano-r-4a,c-5,c-8,c-8a-tetrahydro-4H-3,1-benzoxazine 
• 87768-84-1 5,8-methano-2-(p-chlorophenyl)-r-4a,t-5,t-8,c-8a-tetrahydro-4H-3,1-benzoxazine 
• 105879-74-1 2-(4-chlorophenyl)-4ar,5c,8c,8ac-tetrahydro-5,8-methano-4(3H)-quinazolinone 
• 105786-48-9 2-(4-chlorophenyl)-4ar,5t,8t,8ac-tetrahydro-5,8-methano-4(3H)-quinazolinone 
• 105879-70-7 2-(4-chlorophenyl)-4ar,5c,6,7,8c,8ac-hexahydro-5,8-methano-4(3H)-quinazolinone 
• 105786-44-5 2-(4-chlorophenyl)-4ar,5t,6,7,8t,8ac-hexahydro-5,8-methano-4(3H)-quinazolinone 
• 94098-57-4 (1S,2R,7R,8R)-4-(4-Chloro-phenyl)-3-oxa-5-aza-tricyclo[6.2.1.0^2,7]undec-4-ene 

Relevant articles and documents

Sequential C-H activation enabled expedient delivery of polyfunctional arenes

Modular construction of polyfunctional arenes from abundant feedstocks stands as an unremitting pursue in synthetic chemistry, accelerating the discovery of drugs and materials. Herein, using the multiple C-H activation strategy with versatile imidate esters, the expedient delivery of molecular libraries of densely functionalized sulfur-containing arenes was achieved, which enabled the concise construction of biologically active molecules, such as Bipenamol.

Synthesis of Highly Fused Pyrano[2,3- b]pyridines via Rh(III)-Catalyzed C-H Activation and Intramolecular Cascade Annulation under Room Temperature

A facile access to the polycyclic-fused pyrano[2,3-b]pyridines has been established under room temperature via Rh(III)-catalyzed C-H bond activation and intramolecular cascade annulation. This strategy features high efficiency, unique versatility, and gen

Rhodium-Catalyzed Relay Carbenoid Functionalization of Aromatic C-H Bonds toward Fused Heteroarenes

A rhodium-catalyzed annulation between ethyl benzimidates and α- aroyl sulfur ylides was developed, affording a series of pyrano[4,3,2-ij]isoquinoline derivatives in moderate to good yields with good functional group compatibility. The procedure featured