1262306-22-8

Basic information

• Product Name: benzyloxycarbonylamino-4-chlorobenzoate
• Synonyms: benzyloxycarbonylamino-4-chlorobenzoate
• CAS NO: 1262306-22-8
• Molecular Weight: 305.718
• Mol File: 1262306-22-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: benzyloxycarbonylamino-4-chlorobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyloxycarbonylamino-4-chlorobenzoate(1262306-22-8)
• EPA Substance Registry System: benzyloxycarbonylamino-4-chlorobenzoate(1262306-22-8)

Safety Data

• Hazardous Substances Data: 1262306-22-8(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 3426-71-9 Benzyl N-hydroxycarbamate 
• 122-01-0 4-chloro-benzoyl chloride 

Downstream Products

• 67341-08-6 (+/-)-benzyl 2-hydroxy-2-phenylethylcarbamate 
• 67553-20-2 (+/-)-benzyl 2-hydroxy-1-phenylethylcarbamate 
• 6372-14-1 (2S)-2-(N-benzyloxycarbonyl)-amino-3-phenyl propanol 
• 1262306-34-2 benzyl (+)-(3S,4R)-3-(benzyloxycarbonylamino)-4-hydroxypyrrolidine-1-carboxylate 
• 1262306-33-1 benzyl (-)-(3R,4S)-3-(benzyloxycarbonylamino)-4-hydroxypyrrolidine-1-carboxylate 
• 1262306-43-3 benzyl 1-(diethoxyphosphoryl)-3-hydroxypropan-2-ylcarbamate 
• 888716-49-2 (+)-(2R,3S)-isopropyl 3-(benzyloxycarbonylamino)-2-hydroxy-3-phenylpropanoate 
• 1054314-37-2 (-)-(2S,3R)-isopropyl 3-(benzyloxycarbonylamino)-2-hydroxy-3-phenylpropanoate 
• 207396-23-4 (2R,3S)-N-benzyloxycarbonyl-3-phenylserine methyl ester 
• 207396-31-4 (2S,3R)-N-benzyloxycarbonyl-3-phenylserine methyl ester 
• 92645-06-2 (+/-)-cis-benzyl N-(2-hydroxycyclohexyl)carbamate 
• 1353743-62-0 benzyl (2,4-dihydroxy-2-methylbutyl)carbamate 

Relevant articles and documents

Chemoenzymatic Synthesis and Pharmacological Characterization of Functionalized Aspartate Analogues As Novel Excitatory Amino Acid Transporter Inhibitors

Aspartate (Asp) derivatives are privileged compounds for investigating the roles governed by excitatory amino acid transporters (EAATs) in glutamatergic neurotransmission. Here, we report the synthesis of various Asp derivatives with (cyclo)alkyloxy and (

IMPROVED AMINOHYDROXYLATION OF ALKENES

The invention relates to a process for the aminohydroxylation of alkenes using N-oxycarbamate reagents, e.g. N-acyloxycarbamate, N-alkyloxycarbonyloxycarbamate and N-aralkoxycarbonyloxycarbamate reagents. The invention particularly relates to an intermolecular aminohydroxylation reaction that can be carried out in the absence of added base. The invention also relates to novel N-oxycarbamate reagents that are stable crystalline materials. The process of the invention is useful in the synthesis of compounds having a vicinal amino alcohol moiety, such as biologically active compounds.