861821-42-3

Basic information

• Product Name: 2-Thiazolidinone, 4-[(2E,5R,8S)-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-8-methyl-1-oxo-2- undecen-9-ynyl]-3-[(4-methoxyphenyl)methyl]-, (4R)-
• CAS NO: 861821-42-3
• Molecular Formula: C29H43NO4SSi
• Molecular Weight: 529.816
• Mol File: 861821-42-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Thiazolidinone, 4-[(2E,5R,8S)-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-8-methyl-1-oxo-2- undecen-9-ynyl]-3-[(4-methoxyphenyl)methyl]-, (4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Thiazolidinone, 4-[(2E,5R,8S)-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-8-methyl-1-oxo-2- undecen-9-ynyl]-3-[(4-methoxyphenyl)methyl]-, (4R)-(861821-42-3)
• EPA Substance Registry System: 2-Thiazolidinone, 4-[(2E,5R,8S)-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-8-methyl-1-oxo-2- undecen-9-ynyl]-3-[(4-methoxyphenyl)methyl]-, (4R)-(861821-42-3)

Safety Data

• Hazardous Substances Data: 861821-42-3(Hazardous Substances Data)

Upstream product

• 861821-43-4 dimethyl 2-((R)-3-(4-methoxybenzyl)-2-oxothiazolidin-4-yl)-2-oxoethyl-phosphonate 
• 646994-44-7 (3R,6S)-3-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-non-7-ynal 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 101860-50-8 (-)-3-(4-methoxybenzyl)-2-oxo-thiazolidine-4-carboxylic acid ethyl ester 
• 646994-43-6 ((1R,4S)-1-Allyl-4-methyl-hept-5-ynyloxy)-tert-butyl-dimethyl-silane 
• 824-94-2 p-methoxybenzyl chloride 
• 2746-25-0 p-Methoxybenzyl bromide 

Downstream Products

• 928112-44-1 (Z)-3-Methyl-oct-2-en-6-ynoic acid (2R,4R,6R)-2-methoxy-2-[(R)-3-(4-methoxy-benzyl)-2-oxo-thiazolidin-4-yl]-6-((S)-3-methyl-hex-4-ynyl)-tetrahydro-pyran-4-yl ester 
• 646994-51-6 (R)-3-(4-Methoxy-benzyl)-4-((Z)-(1R,10S,13R,15R)-15-methoxy-5,10-dimethyl-3-oxo-2,14-dioxa-bicyclo[11.3.1]heptadec-4-en-8-yn-15-yl)-thiazolidin-2-one 
• 1053714-70-7 Trifluoro-methanesulfonic acid (2R,4S,6R)-2-methoxy-2-[(R)-3-(4-methoxy-benzyl)-2-oxo-thiazolidin-4-yl]-6-((S)-3-methyl-hex-4-ynyl)-tetrahydro-pyran-4-yl ester 
• 646994-49-2 (R)-4-[(2R,4S,6R)-4-Hydroxy-2-methoxy-6-((S)-3-methyl-hex-4-ynyl)-tetrahydro-pyran-2-yl]-3-(4-methoxy-benzyl)-thiazolidin-2-one 
• 101915-87-1 6,7-(Z)-N-PMB-15-OMe-Latrunculin B 
• 76343-94-7 latrunculin B 
• 76343-93-6 latrunculin A 
• 861821-49-0 (2Z,6E)-3-Methyl-deca-2,6-dien-8-ynoic acid (2R,4R,6R)-2-methoxy-2-[(R)-3-(4-methoxy-benzyl)-2-oxo-thiazolidin-4-yl]-6-((S)-3-methyl-hex-4-ynyl)-tetrahydro-pyran-4-yl ester 
• 928112-42-9 4-[2,4-dihydroxy-6-(3-methyl-hex-4-ynyl)-tetrahydro-pyran-2-yl]-3-(4-methoxy-benzyl)-thiazolidin-2-one 
• 646994-48-1 4-[2,4-dihydroxy-6-(3-methyl-hex-4-ynyl)-tetrahydro-pyran-2-yl]-3-(4-methoxy-benzyl)-thiazolidin-2-one 

Relevant articles and documents

Concise and practical synthesis of latrunculin A by ring-closing enyne-yne metathesis

(Chemical Equation Presented) Selective actin-binding is the most prominent biochemical property of the scarce marine natural product latrunculin A (see formula). Modern metal-catalyzed C-C bond-formation reactions, including a ring-closing enyne-yne metathesis (shown in red), now open a convenient, flexible, and productive entry to this important probe molecule for chemical biology.