3182-77-2

Usage

Uses

Used in Pharmaceutical Industry:
ALLYLAMINO-ACETIC ACID HYDROCHLORIDE is used as a chemical intermediate for the synthesis of various drugs, particularly angiotensin-converting enzyme (ACE) inhibitors.
Used in Cardiovascular Disease Treatment:
ALLYLAMINO-ACETIC ACID HYDROCHLORIDE is used as a precursor in the development of pharmaceuticals for the treatment of cardiovascular diseases and hypertension.
Used in Chemical Research and Development:
ALLYLAMINO-ACETIC ACID HYDROCHLORIDE is used as a building block for the synthesis of other organic compounds, contributing to the advancement of chemical research and development.

InChI:InChI=1/C5H9NO2/c1-2-3-6-4-5(7)8/h2,6H,1,3-4H2,(H,7,8)

Upstream product

• 3182-79-4 N-allylglycine ethyl ester 
• 79-11-8 chloroacetic acid 
• 107-11-9 1-amino-2-propene 
• 79-07-2 Chloroacetamide 
• 105-36-2 ethyl bromoacetate 
• 10552-80-4 N-allylglycine methyl ester 

Downstream Products

• 222725-35-1 N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-2-propen-1-yl-glycine 
• 51858-20-9 3-allylsydnone 
• 127474-54-8 (R)-2-(benzyloxycarbonylamino)pent-4-enoic acid 
• 894401-54-8 2-(2,6-dichlorobenzamido)pent-4-enoic acid 
• 894401-77-5 (S)-2-(2,6-dichlorobenzamido)pent-4-enoic acid 
• 894401-62-8 2-(2,6-difluorobenzamido)pent-4-enoic acid 
• 119479-32-2 2-((tert-butyloxycarbonyl)amino)-4-pentenoic acid 
• 1463484-59-4 tert-butyl-6a-phenyl-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]isoxazole-5-carboxylate 
• 1463484-70-9 tert-butyl 3-amino-4-(hydroxymethyl)-3-phenyl-pyrrolidine-1-carboxylate 
• 1463484-89-0 tert-butyl-1-(benzoylcarbamothioyl)-6a-phenyl-3,3a,4,6-tetrahydropyrrolo[3,4-c]isoxazole-5-carboxylate 
• 1463484-90-3 tert-butyl 1-(benzoylcarbamothioyl)-6a-(2-thienyl)-3,3a,4,6-tetrahydropyrrolo[3,4-c]isoxazole-5-carboxylate 
• 1463484-92-5 tert-butyl 6a-isothiazol-5-yl-1-[(4-methoxyphenyl)methyl]-3,3a,4,6-tetrahydropyrrolo[3,4-c]isoxazole-5-carboxylate 
• 1463484-93-6 tert-butyl 3-amino-4-(hydroxymethyl)-3-isothiazol-5-yl-pyrrolidine-1-carboxylate 
• 1463484-94-7 tert-butyl 3-(benzoylcarbamothioylamino)-4-(hydroxymethyl)-3-phenyl-pyrrolidine-1-carboxylate 

Relevant academic research and scientific papers

TETRAHYDROPYRROLOTHIAZINE COMPOUNDS

The present invention provides compounds of Formula I: wherein A is selected from the group consisting of; R1 is H or F; R2 is H, —CH2OH, C1-C3 alkyl, R3 is H, F, or CN; R4 is H, F; or CN; and R5 is H, —CH3, or —OCH3; or a pharmaceutically acceptable salt thereof.

Cross-metathesis of N-alkenyl peptoids with O- or C-allyl glycosides

Cross-metathesis of several N-alkenyl-containing oligoglycines derivatives (peptoids) with protected O or C-allyl glycosides of N- acetylglucosamine, galactose, and mannose using Grubbs' ruthenium benzylidene catalyst (Cy3P)2Cl2Ru=CHPh (1) has been achieved in 40 to 52% yields.

Synthesis and reactions of 9,10-diazatetracyclo-[6.3.0.0.4,110.5.9]undecanes

The tandem 1,3-dipolar cycloaddition between sydnones and 1,5-cyclooctadiene provides 9,10-diazatetracyclo[6.3.0.0.4,110.5,9]undecanes (the Weintraub reaction) in modest to good yields.