923748-45-2

Basic information

• Product Name: N-(pyridin-2-yl)monomethyl terephthalate monoamide
• Synonyms: N-(pyridin-2-yl)monomethyl terephthalate monoamide
• CAS NO: 923748-45-2
• Molecular Weight: 256.261
• Mol File: 923748-45-2.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: N-(pyridin-2-yl)monomethyl terephthalate monoamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(pyridin-2-yl)monomethyl terephthalate monoamide(923748-45-2)
• EPA Substance Registry System: N-(pyridin-2-yl)monomethyl terephthalate monoamide(923748-45-2)

Safety Data

• Hazardous Substances Data: 923748-45-2(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 7377-26-6 4-Methoxycarbonylbenzoyl chloride 
• 462-08-8 pyridin-3-ylamine 
• 3034-86-4 4-ethynylbenzoic acid methyl ester 
• 7364-20-7 4-ethyl-benzoic acid methyl ester 
• 15226-74-1 dicobalt octacarbonyl 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 4589-12-2 N-(pyrid-2-yl)benzamide 
• 5223-01-8 2-phenyl-N-(pyridin-2-yl)acetamide 
• 96354-74-4 N-(diphenylmethyl)pyridin-2-amine 
• 74037-48-2 N-(1,2-diphenylethyl)pyridin-2-amine 
• 1571-08-0 methyl 4-formylbenzoate 
• 42967-55-5 monomethyl monopotassium terephthalate 
• 120-61-6 1,4-benzenedicarboxylic acid dimethyl ester 

Downstream Products

• 1420477-60-6 4-{8-amino-3-[(2S)-1-(1-oxo-2-butyn-1-yl)pyrrolidin-2-yl]imidazo[1,5-a]pyrazin-1-yl}-N-(pyridin-2-yl)benzamide 
• 51484-40-3 N-pyridin-2-yl(1,1'-biphenyl)-4-acetamide 
• 86847-59-8 2-(pivaloylamino)pyridine 
• 74037-48-2 N-(1,2-diphenylethyl)pyridin-2-amine 
• 59898-94-1 N-(pyridin-2-yl)isonicotinamide 
• 14547-82-1 4-chloro-N-(pyridine-2-yl)benzamide 

Relevant articles and documents

Direct Transformation of Alkylarenes into N-(Pyridine-2-yl)amides by C(sp3)–C(sp3) Bond Cleavage

C(sp3)–H bond functionalization and C(sp3)–C(sp3) bond cleavage are very challenging transformations in chemistry. Herein, we report a mild and green methodology for the construction of N-(pyridine-2-yl)amides via tandem C(sp3)–H activation/C–C bond cleavage of alkylarenes. Various N-heterocyclic amides were directly synthesized from alkylarenes in water in moderate to good yields.

Ruthenium-Catalyzed Reductive Arylation of N-(2-Pyridinyl)amides with Isopropanol and Arylboronate Esters

A new three-component reductive arylation of amides with stable reactants (iPrOH and arylboronate esters), making use of a 2-pyridinyl (Py) directing group, is described. The N-Py-amide substrates are readily prepared from carboxylic acids and PyNH2, and the resulting N-Py-1-arylalkanamine reaction products are easily transformed into the corresponding chlorides by substitution of the HN-Py group with HCl. The 1-aryl-1-chloroalkane products allow substitution and cross-coupling reactions. Therefore, a general protocol for the transformation of carboxylic acids into a variety of functionalities is obtained. The Py-NH2 by-product can be recycled.

Copper(i)-catalysed oxidative C-N coupling of 2-aminopyridine with terminal alkynes featuring a CC bond cleavage promoted by visible light

Facile visible-light promoted copper-catalyzed aerobic oxidative C-N coupling between 2-aminopyridine and terminal alkynes at room temperature via CC triple bond cleavage is described. This reaction allows direct synthesis of biologically important pyridy