627099-18-7

Basic information

• Product Name: 4-(3-formylphenoxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester
• Synonyms: 4-(3-formylphenoxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester
• CAS NO: 627099-18-7
• Molecular Weight: 335.4
• Mol File: 627099-18-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-(3-formylphenoxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3-formylphenoxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester(627099-18-7)
• EPA Substance Registry System: 4-(3-formylphenoxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester(627099-18-7)

Safety Data

• Hazardous Substances Data: 627099-18-7(Hazardous Substances Data)

Upstream product

• 108149-63-9 4-hydroxymethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 100-83-4 meta-hydroxybenzaldehyde 
• 95715-86-9 (S)-2,2-dimethyl-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 4-methyl ester 
• 2766-43-0 N-tert-butyloxycarbonyl-L-serine methyl ester 
• 3262-72-4 (S)-N-(tert-butoxycarbonyl)serine 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 627099-30-3 [2-(3-formylphenoxy)-1-(hydroxymethyl)ethyl]carbamic acid tert-butyl ester 

Relevant articles and documents

Synthesis of 3-Aminochroman Derivatives by Radical Cyclization

(Equation presented) Enantiomerically pure 5-acetyl-3-amino-3,4-dihydro-2H- 1-benzopyran and methyl 3-amino-3,4-dihydro-2H-1-benzopyran-5-carboxylate were successfully synthesized starting from D- or L-serine. The formation of the benzopyran ring involved a radical cyclization step. The enantiomeric purities of the final aminochroman derivatives were determined by capillary electrophoresis using β-cyclodextrins as a chiral selector.