19396-05-5

Basic information

• Product Name: (3S,4S)-5-(carbamoyloxy)-3,4-dihydroxy-L-norvaline
• CAS NO: 19396-05-5
• Molecular Formula: C₆H₁₂N₂O₆
• Molecular Weight: 208.1693
• Mol File: 19396-05-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 642.9°C at 760 mmHg
• Flash Point: 342.6°C
• Density: 1.611g/cm³
• Vapor Pressure: 3.07E-19mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: (3S,4S)-5-(carbamoyloxy)-3,4-dihydroxy-L-norvaline(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4S)-5-(carbamoyloxy)-3,4-dihydroxy-L-norvaline(19396-05-5)
• EPA Substance Registry System: (3S,4S)-5-(carbamoyloxy)-3,4-dihydroxy-L-norvaline(19396-05-5)

Safety Data

• Hazardous Substances Data: 19396-05-5(Hazardous Substances Data)

Upstream product

• 52471-73-5 (2S,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxycarbonylamino-5-carbamoyloxy-pentanoic acid 
• 22886-47-1 (2S,4R)-2-Amino-5-carbamoyloxy-4-hydroxy-pentanoic acid 
• 105281-26-3 N-[(S)-1-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-allyl]-4-chloro-benzamide 
• 152390-97-1 N-Benzyl-N-[(S)-((4S,5S)-5-benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-furan-2-yl-methyl]-hydroxylamine 
• 152390-99-3 [(S)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-furan-2-yl-methyl]-carbamic acid tert-butyl ester 
• 152391-01-0 [(S)-((4S,5S)-5-Carbamoyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-furan-2-yl-methyl]-carbamic acid tert-butyl ester 
• 90661-54-4 (3S,4S)-5-<(aminocarbonyl)oxy>-N-<(1,1-dimethylethoxy)carbonyl>-3,4-<(1-methylethylidene)dioxy>-D-norvaline 
• 37362-29-1 polyoxin N 
• 90661-54-4 5-O-(aminocarbonyl)-2-[((1,1-dimethylethyl)oxycarbonyl)amino]-2-deoxy-3,4-O-(1-methylethylidene)-L-xylonic acid 
• 52471-68-8 (2S,3S,4S)-2-Azido-3,4-bis-benzyloxy-5-carbamoyloxy-pentanoic acid 
• 152391-00-9 (1S)-1-(tert-butoxycarbonylamino)-1-deoxy-1-(2-furyl)-2,3-O-isopropylidene-L-threitol 

Relevant articles and documents

The structures of polyoxins A and B.

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A concise synthesis of (+)-polyoxamic acid and (+)-5-O-carbamoyl polyoxamic acid

We report the concise synthesis of (+)-polyoxamic acid and (+)-5-O-carbamoyl polyoxamic acid from L-xylose in seven or six steps, respectively. The key steps include a diastereoselective amination of syn-1,2-polybenzyl ethers using chlorosulfonyl isocyanate (CSI) and the one-pot introduction of carbamates into the allylic benzyl ether and primary hydroxyl moieties. Georg Thieme Verlag Stuttgart.

A Convenient Synthesis of Polyoxamic Acid, 5-O-Carbamoylpolyoxamic Acid, and Their Unnantural D Isomers

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