86235-37-2

Basic information

• Product Name: Dicarbobenzoxy-allohydroxylysin-δ-lacton
• CAS NO: 86235-37-2
• Molecular Weight: 412.442
• Mol File: 86235-37-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Dicarbobenzoxy-allohydroxylysin-δ-lacton(CAS DataBase Reference)
• NIST Chemistry Reference: Dicarbobenzoxy-allohydroxylysin-δ-lacton(86235-37-2)
• EPA Substance Registry System: Dicarbobenzoxy-allohydroxylysin-δ-lacton(86235-37-2)

Safety Data

• Hazardous Substances Data: 86235-37-2(Hazardous Substances Data)

Upstream product

• 96261-29-9 dicarbobenzoxy-δ-hydroxy-L-lysine-lactone 
• 79432-05-6 ε-carbobenzoxy-δ-hydroxy-L-lysine (normal and allo forms) 
• 501-53-1 benzyl chloroformate 
• 96359-88-5 (2S,5S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-5-hydroxy-hexanoic acid 
• 144090-63-1 (2S,5S)-6-Azido-5-benzyloxy-2-tert-butoxycarbonylamino-hexanoic acid 
• 144090-61-9 (S)-4-((S)-4-Azido-3-benzyloxy-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 144090-62-0 ((1S,4S)-5-Azido-4-benzyloxy-1-hydroxymethyl-pentyl)-carbamic acid tert-butyl ester 
• 144090-59-5 (S)-4-((S)-4-Azido-3-hydroxy-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 144090-58-4 (S)-2,2-Dimethyl-4-(2-oxiranyl-ethyl)-oxazolidine-3-carboxylic acid tert-butyl ester 
• 144090-57-3 tert-butyl (S)-4-(but-3-enyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 79432-05-6 L_S-threo-2-amino-6-benzyloxycarbonylamino-5-hydroxy-hexanoic acid 

Downstream Products

• 75466-94-3 ((2S,5S)-2,6-Bis-benzyloxycarbonylamino-5-hydroxy-hexanoylamino)-acetic acid tert-butyl ester 
• 75466-94-3 ((2S,5R)-2,6-Bis-benzyloxycarbonylamino-5-hydroxy-hexanoylamino)-acetic acid tert-butyl ester 
• 75466-98-7 {(2R,5S)-2,6-Bis-benzyloxycarbonylamino-5-[(2S,3S,4R,5R,6S)-4,5-diacetoxy-6-acetoxymethyl-3-((2S,3S,4R,5S,6S)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoylamino}-acetic acid tert-butyl ester 
• 75466-99-8 {(2R,5S)-2,6-Bis-benzyloxycarbonylamino-5-[(2S,3S,4R,5R,6S)-4,5-diacetoxy-6-acetoxymethyl-3-((2S,3S,4R,5S,6S)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoylamino}-acetic acid 
• 75477-74-6 {(2S,5R)-2,6-Bis-benzyloxycarbonylamino-5-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-hydroxymethyl-3-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoylamino}-acetic acid 
• 75466-96-5 4-Oxo-pentanoic acid (2S,3S,4R,5R,6S)-4,5-diacetoxy-6-acetoxymethyl-2-[(1S,4R)-4-benzyloxycarbonylamino-1-(benzyloxycarbonylamino-methyl)-4-(tert-butoxycarbonylmethyl-carbamoyl)-butoxy]-tetrahydro-pyran-3-yl ester 
• 75466-97-6 [(2R,5S)-2,6-Bis-benzyloxycarbonylamino-5-((2S,3S,4S,5R,6S)-4,5-diacetoxy-6-acetoxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-hexanoylamino]-acetic acid tert-butyl ester 
• 115829-38-4 (+/-)-erythro-2,6-bis-benzyloxycarbonylamino-5-hydroxy-hexanoic acid hydrazide 
• 113455-38-2 (+/-)-erythro-2,6-bis-benzyloxycarbonylamino-5-hydroxy-hexanoic acid amide 
• 504-91-6 DL-erythro-5-hydroxy-lysine 
• 75466-98-7 {(2R,5R)-2,6-Bis-benzyloxycarbonylamino-5-[(2S,3S,4R,5R,6S)-4,5-diacetoxy-6-acetoxymethyl-3-((2S,3S,4R,5S,6S)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoylamino}-acetic acid tert-butyl ester 
• 75466-99-8 {(2R,5R)-2,6-Bis-benzyloxycarbonylamino-5-[(2S,3S,4R,5R,6S)-4,5-diacetoxy-6-acetoxymethyl-3-((2S,3S,4R,5S,6S)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoylamino}-acetic acid 
• 75477-74-6 {(2S,5S)-2,6-Bis-benzyloxycarbonylamino-5-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-hydroxymethyl-3-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoylamino}-acetic acid 
• 75466-96-5 4-Oxo-pentanoic acid (2S,3S,4R,5R,6S)-4,5-diacetoxy-6-acetoxymethyl-2-[(1R,4R)-4-benzyloxycarbonylamino-1-(benzyloxycarbonylamino-methyl)-4-(tert-butoxycarbonylmethyl-carbamoyl)-butoxy]-tetrahydro-pyran-3-yl ester 

Relevant articles and documents

A Strategy Towards the Stereoselective Synthesis of 5-Hydroxylysine

A stereoselective synthesis of 5-hydroxylysine is described in which the α-stereogenic centre is generated by a Schoellkopf amino acid synthesis, and the ethanolamine structure is obtained via Sharpless aminohydroxylation from an olefin moiety. The reactions and their selectivities are studied.

SYNTHESIS OF O-(2-O-α-D-GLUCOPYRANOSYL)-β-D-GALACTOPYRANOSIDE OF OPTICALLY PURE δ-HYDROXY-L-LYSYLGLYCINE AND δ-HYDROXY-L-LYSYLGLYCYL-L-GLUTAMYL-L-ASPARATYLGLYCINE. COMPONENTS OF THE GLOMERULAR BASEMENT MEMBRANE

The application of the levulinyl group as a temporary blocking group for the 2-OH function of galactose proved to be very efficient not only for the introduction of a β- linkage between galactose and the optically pure δ-hydroxy-L-lysylglycine, but also t