120385-97-9

Basic information

• Product Name: 3-((2-Carbamoylmethoxycarbonyl-ethylsulfanyl)-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-methylsulfanyl)-propionic acid carbamoylmethyl ester
• Synonyms: 3-((2-Carbamoylmethoxycarbonyl-ethylsulfanyl)-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-methylsulfanyl)-propionic acid carbamoylmethyl ester
• CAS NO: 120385-97-9
• Molecular Weight: 602.132
• Mol File: 120385-97-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-((2-Carbamoylmethoxycarbonyl-ethylsulfanyl)-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-methylsulfanyl)-propionic acid carbamoylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-((2-Carbamoylmethoxycarbonyl-ethylsulfanyl)-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-methylsulfanyl)-propionic acid carbamoylmethyl ester(120385-97-9)
• EPA Substance Registry System: 3-((2-Carbamoylmethoxycarbonyl-ethylsulfanyl)-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-methylsulfanyl)-propionic acid carbamoylmethyl ester(120385-97-9)

Safety Data

• Hazardous Substances Data: 120385-97-9(Hazardous Substances Data)

Upstream product

• 120385-96-8 dimethyl 5-<3-<2-(7-chloro-2-quinolinyl)-(E)-ethenyl>phenyl>-4,6-dithianonanedioate 
• 683-57-8 bromo-acetic acid amide 
• 120386-00-7 5-(3-(2-(7-CHLOROQUINOLIN-2-YL)ETHENYL)PHENYL)-4,6-DITHIANONANEDIOIC ACID 

Downstream Products

• 120386-00-7 5-(3-(2-(7-CHLOROQUINOLIN-2-YL)ETHENYL)PHENYL)-4,6-DITHIANONANEDIOIC ACID 
• 120385-99-1 (S)-3-(((3-(2-(7-chloroquinolin-2-yl)-(E)-ethenyl)phenyl)((3-((aminocarbonyl)methoxy)-3-oxopropyl)thio)methyl)thio)propionic acid 
• 120385-99-1 3-((R)-(2-Carbamoylmethoxycarbonyl-ethylsulfanyl)-{3-[(E)-2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-methylsulfanyl)-propionic acid 

Relevant articles and documents

Lipase-Catalyzed Asymmetric Hydrolysis of Esters Having Remote Chiral/Prochiral Centers

Enzymatic hydrolysis of prochiral and racemic dithioacetal esters having up to five bonds between the prochiral/chiral center and the ester carbonyl group proceeds with selectivities up to 98 percent enantiomeric excess when commercially available lipases