482620-97-3

Basic information

• Product Name: (R)-2-Dec-9-ynyloxy-3-(4-methoxy-benzyloxy)-propan-1-ol
• Synonyms: (R)-2-Dec-9-ynyloxy-3-(4-methoxy-benzyloxy)-propan-1-ol
• CAS NO: 482620-97-3
• Molecular Weight: 348.483
• Mol File: 482620-97-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-2-Dec-9-ynyloxy-3-(4-methoxy-benzyloxy)-propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-Dec-9-ynyloxy-3-(4-methoxy-benzyloxy)-propan-1-ol(482620-97-3)
• EPA Substance Registry System: (R)-2-Dec-9-ynyloxy-3-(4-methoxy-benzyloxy)-propan-1-ol(482620-97-3)

Safety Data

• Hazardous Substances Data: 482620-97-3(Hazardous Substances Data)

Upstream product

• 109786-73-4 (S)-4-[(4-methoxybenzyloxy)methyl]-2,2-dimethyl-1,3-dioxolane 
• 824-94-2 p-methoxybenzyl chloride 
• 119227-71-3 9-decynyl mesylate 
• 220641-23-6 1-O-(triphenylmethyl)-3-O-(4'-methoxybenzyl)-sn-glycerol 
• 109786-74-5 (R)-3-(4-methoxybenzyloxy)propane-1,2-diol 
• 482620-96-2 1-((S)-2-Dec-9-ynyloxy-3-trityloxy-propoxymethyl)-4-methoxy-benzene 

Downstream Products

• 482621-06-7 C₇₃H₉₈O₇ 
• 482621-12-5 C₇₃H₉₈O₇ 
• 482621-19-2 1-{(R)-3-Dec-9-ynyloxy-2-[20-((S)-2-dec-9-ynyloxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-propoxymethyl}-4-methoxy-benzene 
• 482621-16-9 1-{(R)-3-Dec-9-ynyloxy-2-[20-((R)-2-dec-9-ynyloxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-propoxymethyl}-4-methoxy-benzene 
• 486403-27-4 C₆₂H₉₂O₈ 
• 486403-24-1 C₆₂H₉₄O₈ 
• 486403-21-8 (S)-2-{20-[(R)-1-Hydroxymethyl-2-(4-methoxy-benzyloxy)-ethoxy]-icosa-9,11-diynyloxy}-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 482621-11-4 (R)-2-[20-((S)-2-Hydroxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 482621-05-6 (R)-2-[20-((R)-2-Hydroxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-3-(4-methoxy-benzyloxy)-propan-1-ol 

Relevant articles and documents

Efficient synthesis of parallel cyclobolaphiles having two diacetylenes: Mimetics of archaeal membrane lipids

Chiral 48-membered parallel cyclobolaphiles and their diastereomer having two diacetylenes were efficiently synthesized by utilizing both the selective deprotection and the cross-coupling method of two distinct acetylenic compounds.