121683-04-3

Basic information

• Product Name: 4-(benzyloxy)butyl methanesulfonate
• Synonyms: 4-(benzyloxy)butyl methanesulfonate
• CAS NO: 121683-04-3
• Molecular Weight: 258.339
• Mol File: 121683-04-3.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 4-(benzyloxy)butyl methanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(benzyloxy)butyl methanesulfonate(121683-04-3)
• EPA Substance Registry System: 4-(benzyloxy)butyl methanesulfonate(121683-04-3)

Safety Data

• Hazardous Substances Data: 121683-04-3(Hazardous Substances Data)

Upstream product

• 4541-14-4 4-benzyloxy-butan-1-ol 
• 124-63-0 methanesulfonyl chloride 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 

Downstream Products

• 121683-05-4 9-(4'-benzyloxybutyl) adenine 
• 50873-94-4 (4-iodobutoxymethyl)benzene 
• 1354382-57-2 (S)-4-((4-(benzyloxy)butoxy)methyl)-2,2-dimethyl-1,3-dioxolane 
• 1332392-73-0 (4-(benzyloxy)butyl)(4,4,5,5,5-pentafluoropentyl)sulfane 
• 60789-54-0 4-bromobutyl benzyl ether 
• 915213-60-4 C₁₆H₂₄O₂ 
• 201289-53-4 (8-Benzyloxy-oct-3-ynyloxy)-tert-butyl-dimethyl-silane 
• 1026688-08-3 toluene-4-sulfonic acid 6-benzyloxy-2-hydroxymethyl-hexyl ester 
• 151134-32-6 diethyl 2-(4-(benzyloxy)butyl)malonate 
• 151134-33-7 2-(4-(benzyloxy)butyl)propane-1,3-diol 
• 1026980-57-3 3-(4-(benzyloxy)butyl)oxetane 
• 42729-95-3 4-hydroxybutyl methanesulfonate 

Relevant articles and documents

4-Methanesulfonyloxybutanol: hydrolysis of busulfan.

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Stereoselective Synthesis of Conjugated Polyenes Based on Tethered Olefin Metathesis and Carbonyl Olefination: Application to the Total Synthesis of (+)-Bretonin B

The combination of a highly stereoselective tethered olefin metathesis reaction and a Julia-Kocienski olefination is presented as a strategy for the synthesis of conjugated polyenes with at least one Z-configured Ca?C bond. The strategy is exemplified by the synthesis of the marine natural product (+)-bretonin B.

Indol-3-ylcycloalkyl ketones: Effects of N1 substituted indole side chain variations on CB2 cannabinoid receptor activity

Several 3-acylindoles with high affinity for the CB2 cannabinoid receptor and selectivity over the CB1 receptor have been prepared. A variety of 3-acyl substituents were investigated, and the tetramethylcyclopropyl group was found to lead to high affinity CB2 agonists (5, 16). Substitution at the N1-indole position was then examined. A series of aminoalkylindoles was prepared and several substituted aminoethyl derivatives were active (23-27, 5) at the CB2 receptor.Astudy of N1 nonaromatic side chain variants provided potent agonists at the CB2 receptor (16, 35-41, 44-47, 49-54, and 57-58). Several polar side chains (alcohols, oxazolidinone) were well-tolerated for CB2 receptor activity (41, 50), while others (amide, acid) led to weaker or inactive compounds (55 and 56). N1 aromatic side chains also afforded several high affinity CB2 receptor agonists (61, 63, 65, and 69) but were generally less potent in an in vitro CB2 functional assay than were nonaromatic side chain analogues.