856676-69-2

Basic information

• Product Name: Benzoic acid (2S,5R)-5-{5-[3-(6-{3-[4-chloro-3-(3-methyl-but-2-enyloxy)-phenylcarbamoyl]-furan-2-yl}-hexyloxy)-prop-1-ynyl]-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl}-2,5-dihydro-furan-2-ylmethyl ester
• Synonyms: Benzoic acid (2S,5R)-5-{5-[3-(6-{3-[4-chloro-3-(3-methyl-but-2-enyloxy)-phenylcarbamoyl]-furan-2-yl}-hexyloxy)-prop-1-ynyl]-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl}-2,5-dihydro-furan-2-ylmethyl ester
• CAS NO: 856676-69-2
• Molecular Weight: 756.252
• Mol File: 856676-69-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzoic acid (2S,5R)-5-{5-[3-(6-{3-[4-chloro-3-(3-methyl-but-2-enyloxy)-phenylcarbamoyl]-furan-2-yl}-hexyloxy)-prop-1-ynyl]-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl}-2,5-dihydro-furan-2-ylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid (2S,5R)-5-{5-[3-(6-{3-[4-chloro-3-(3-methyl-but-2-enyloxy)-phenylcarbamoyl]-furan-2-yl}-hexyloxy)-prop-1-ynyl]-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl}-2,5-dihydro-furan-2-ylmethyl ester(856676-69-2)
• EPA Substance Registry System: Benzoic acid (2S,5R)-5-{5-[3-(6-{3-[4-chloro-3-(3-methyl-but-2-enyloxy)-phenylcarbamoyl]-furan-2-yl}-hexyloxy)-prop-1-ynyl]-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl}-2,5-dihydro-furan-2-ylmethyl ester(856676-69-2)

Safety Data

• Hazardous Substances Data: 856676-69-2(Hazardous Substances Data)

Upstream product

• 191984-82-4 1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene 
• 191984-84-6 4-chloro-3-(3-methyl-2-butenyloxy)-benzenamine 
• 121-88-0 5-Nitro-2-aminophenol 
• 619-10-3 5-nitro-2-chlorophenol 
• 856676-65-8 2-(6-prop-2-ynyloxy-hexyl)-furan-3-carboxylic acid 
• 856676-64-7 2-(6-prop-2-ynyloxy-hexyl)-furan-3-carboxylic acid methyl ester 
• 856676-68-1 5'-benzoyl-5-iodo-d4T 
• 856676-66-9 2-(6-prop-2-ynyloxy-hexyl)-furan-3-carboxylic acid [4-chloro-3-(3-methyl-but-2-enyloxy)-phenyl]-amide 

Relevant articles and documents

New methodology for 2-alkylation of 3-furoic acids: Application to the synthesis of tethered UC-781/d4T bifunctional HIV reverse-transcriptase inhibitors

New methodology for 2-alkylation of 3-furoic acids is presented involving Wittig reactions of the 3-methoxycarbonyl-2-furanylmethylphosphonium salt. The methodology has been used to prepare a tethered 2-alkylated-UC-781/d4T conjugate as a potentially new type of HIV reverse-transcriptase inhibitor.