75986-04-8

Basic information

• Product Name: benzyl α-(2-oxo-3-methylene-1-azetidinyl)-p-benzyloxyphenylacetate
• Synonyms: benzyl α-(2-oxo-3-methylene-1-azetidinyl)-p-benzyloxyphenylacetate
• CAS NO: 75986-04-8
• Molecular Weight: 413.473
• Mol File: 75986-04-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: benzyl α-(2-oxo-3-methylene-1-azetidinyl)-p-benzyloxyphenylacetate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl α-(2-oxo-3-methylene-1-azetidinyl)-p-benzyloxyphenylacetate(75986-04-8)
• EPA Substance Registry System: benzyl α-(2-oxo-3-methylene-1-azetidinyl)-p-benzyloxyphenylacetate(75986-04-8)

Safety Data

• Hazardous Substances Data: 75986-04-8(Hazardous Substances Data)

Upstream product

• 53249-34-6 N-t-butoxycarbonyl-p-hydroxyphenylglycine 
• 75986-02-6 α-amino-4-(phenylmethoxy)benzeneacetic acid phenylmethyl ester HCl 
• 76023-83-1 benzyl N-t-butoxycarbonyl-p-benzyloxyphenylglycinate 
• 6324-01-2 p-hydroxyphenylglycine 
• 100-39-0 benzyl bromide 
• 201230-82-2 carbon monoxide 
• 75986-03-7 benzyl N-(2-bromo-2-propenyl)-p-benzyloxyphenylglycinate 

Downstream Products

• 68682-19-9 Benzyl (+/-)-(αR^*,3S^*)-3-Amino-α--2-oxo-1-azetidineacetate Hydrotosylate 
• 68682-21-3 Benzyl (+/-)-(αR^*,3R^*)-3-Amino-α--2-oxo-1-azetidineacetate Hydrotosylate 
• 67509-39-1 (+/-)-dibenzyl 3-ANA 
• 67509-39-1 (+/-)-epi-dibenzyl 3-ANA 
• 79644-54-5 benzyl α-(3-hydroxyimino-2-oxo-1-azetidinyl)-p-benzyloxyphenylacetate 
• 79644-53-4 1-<(p-benzyloxyphenyl)benzyloxycarbonylmethyl>azetidine-2,3-dione 
• 75986-12-8 (+/-)-benzyl 3-acetylamino-O-benzylnocardicinate 
• 75986-12-8 (+/-)-epi-benzyl 3-acetylamino-O-benzylnocardicinate 
• 75986-06-0 benzyl α-(3-hydroxy-3-hydroxymethyl-2-oxo-1-azetidinyl)-p-benzyloxyphenylacetate 

Relevant articles and documents

A Novel Synthesis of (+/-)-3-Aminonocardinic Acid

(+/-)-3-Aminonocardinic acid, which is an important starting material for the synthesis of nocardicin A and other biologically active analogues, has been synthesized by application of a new method for synthesis of α-methylene-β-lactams.