104211-10-1

Basic information

• Product Name: [2R-(R*,R*)]-2-hydroxy-3-methoxy-N,N'-bis-(phenylmethoxy)butanediamide
• CAS NO: 104211-10-1
• Molecular Weight: 374.393
• Mol File: 104211-10-1.mol

Chemical Properties

• CAS DataBase Reference: [2R-(R*,R*)]-2-hydroxy-3-methoxy-N,N'-bis-(phenylmethoxy)butanediamide(CAS DataBase Reference)
• NIST Chemistry Reference: [2R-(R*,R*)]-2-hydroxy-3-methoxy-N,N'-bis-(phenylmethoxy)butanediamide(104211-10-1)
• EPA Substance Registry System: [2R-(R*,R*)]-2-hydroxy-3-methoxy-N,N'-bis-(phenylmethoxy)butanediamide(104211-10-1)

Safety Data

• Hazardous Substances Data: 104211-10-1(Hazardous Substances Data)

Upstream product

• 2687-43-6 O-benzylhydoxylamine hydrochloride 
• 104211-02-1 diethyl 2-O-methyl-L-tartrate 
• 98-59-9 p-toluenesulfonyl chloride 
• 104211-08-7 ethyl[2R-(R*,R*)]-2-methoxy-4-oxo-3-hydroxy-4-[(phenylmethoxy)-amino]-butanoate 
• 104211-06-5 Ethyl[2R-(R*,R*)]-2-hydroxy-4-oxo-3-methoxy-4-[(phenylmethoxy)-amino]-butanoate 
• 119770-87-5 (2R,3R)-diethyl 2-(benzyloxy)-3-hydroxysuccinate 
• 124-63-0 methanesulfonyl chloride 
• 104225-96-9 (2R,3R)-2-Hydroxy-3-methoxy-succinic acid 1-ethyl ester 
• 104333-66-6 dimethyl (2R,3R)-2-O-methyltartrate 

Relevant articles and documents

CHIRAL SYNTHESIS OF 3,4-DISUBSTITUTED 2-AZETIDINONES FROM (R,R)-(+)-TARTARIC ACID

A novel route is described for the enantioselective synthesis of 2-azetidinones 24 and 25 from (R,R)-(+)-tartaric acid.Monomethylation, monobenzylation of 2 and the use of site specific pig liver esterase (PLE) to produce 6 and 7 are the key steps in sequ

Synthesis of 3α-alkoxy-4β-substituted-2-azetidinones from L(+)-tartaric acid

Tartaric acid, regioselective saponification, Pig Liver Esterase, 3-methoxy-2-azetidinone, N-Hydroxy-2-thiopyridone, radical decarboxylation. The synthesis of 3α-alkoxy-4β-azetidinones from L(+) tartaric acid is described. Regioselective saponification and methylation along with a stereo selective radical decarboxylative alkylation are key steps leading to optically pure trans-β-lactams.

Optically active 4-carbalkoxy-2-azetidinones

Novel 2-azetidinones of the formula STR1 wherein R is alkyl of 1 to 4 carbon atoms, R1 is selected from the group consisting of hydrogen, --OH, protected hydroxy and --OCH2 --COOR', R' is selected from the group consisting of hydroge