125982-23-2

Basic information

• Product Name: ⁽⁵⁾-tert-butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate
• CAS NO: 125982-23-2
• Molecular Weight: 215.249
• Mol File: 125982-23-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: ⁽⁵⁾-tert-butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: ⁽⁵⁾-tert-butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate(125982-23-2)
• EPA Substance Registry System: ⁽⁵⁾-tert-butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate(125982-23-2)

Safety Data

• Hazardous Substances Data: 125982-23-2(Hazardous Substances Data)

Usage

General Description

⁽⁵⁾-tert-butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate is a chemical compound with the molecular formula C11H19NO4. It is a carbamate derivative with a tert-butyl group attached to the nitrogen atom and a 6-oxotetrahydro-2H-pyran-3-yl moiety. ⁽⁵⁾-tert-butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate is commonly used in organic synthesis as a protecting group for amines and as a reagent in the preparation of various pharmaceuticals and agrochemicals. The tert-butyl group provides steric hindrance and protection for the amine, while the 6-oxotetrahydro-2H-pyran-3-yl moiety can serve as a versatile building block for further chemical transformations. Overall, ⁽⁵⁾-tert-butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate is a valuable compound with diverse applications in the field of organic chemistry.

Upstream product

• 162955-48-8 [(1S)-4-hydroxy-1-(hydroxymethyl)butyl]carbamic acid tert-butyl ester 
• 65487-73-2 (S)-2-((tert-butoxycarbonyl)amino)-5-ethoxy-5-oxopentanoic acid 
• 1119-33-1 (S)-2-Amino-pentanedioic acid 5-ethyl ester 
• 39538-20-0 (S)-2-tert-Butoxycarbonylamino-pentanedioic acid 1-(2,5-dioxo-pyrrolidin-1-yl) ester 5-methyl ester 
• 45214-91-3 (2S)-2-[(tert-butoxy)carbonylamino]-4-(methoxycarbonyl)butanoic acid 
• 24424-99-5 di-tert-butyl dicarbonate 
• 1499-55-4 L-glutamic acid 5-methyl ester 
• 126587-35-7 methyl (4S)-4-[(tert-butoxy)carbonylamino]-5-hydroxypentanoate 
• 125982-19-6 ethyl (4S)-N-(t-butyloxycarbonyl)amino-5-hydroxypentanoate 

Downstream Products

• 133328-98-0 {(3S,4S)-4-[(3-Methoxy-phenyl)-phenylsulfanyl-methyl]-6-oxo-tetrahydro-pyran-3-yl}-carbamic acid tert-butyl ester 
• 133328-98-0 {(3S,4R)-4-[(3-Methoxy-phenyl)-phenylsulfanyl-methyl]-6-oxo-tetrahydro-pyran-3-yl}-carbamic acid tert-butyl ester 
• 133328-97-9 [(3S,4R)-4-(Benzo[1,3]dioxol-5-yl-phenylsulfanyl-methyl)-6-oxo-tetrahydro-pyran-3-yl]-carbamic acid tert-butyl ester 
• 117857-96-2 (2S,3R,4S)-2-(carboxycyclopropyl)glycine 
• 132430-61-6 (2RS,4S)-4-<(tert-butoxycarbonyl)amino>-2-phenylseleno-5-pentanolide 

Relevant articles and documents

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Asymmetric induction in conjugate addition of new chiral γ-heterosubstituted-α, β-unsaturated δ-lactones from L-glutamic acid was accomplished in high diastereoselectivity with the formation of trans-(R,S)-adducts and was disclosed to serve as a versatile procedure for the asymmetric synthesis of antileukemic lignan lactones.