71998-70-4

Basic information

• Product Name: 4-Benzyloxy-1,3-butanediol
• Synonyms: 4-Benzyloxy-1,3-butanediol
• CAS NO: 71998-70-4
• Molecular Formula: C₁₁H₁₆O₃
• Molecular Weight: 196.24
• Mol File: 71998-70-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 75 °C
• Boiling Point: 356.4oC at 760 mmHg
• Flash Point: 169.3oC
• Appearance: /
• Density: 1.13g/cm3
• Vapor Pressure: 1.07E-05mmHg at 25°C
• Refractive Index: 1.54
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Methanol
• CAS DataBase Reference: 4-Benzyloxy-1,3-butanediol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Benzyloxy-1,3-butanediol(71998-70-4)
• EPA Substance Registry System: 4-Benzyloxy-1,3-butanediol(71998-70-4)

Safety Data

• Hazardous Substances Data: 71998-70-4(Hazardous Substances Data)

Usage

General Description

4-Benzyloxy-1,3-butanediol is a chemical compound that belongs to the class of alcohols. It is a colorless, odorless liquid that is soluble in water. This chemical is commonly used in the production of pharmaceuticals, cosmetics, and other industrial applications. It has been studied for its potential medicinal properties, including its use as a precursor in the synthesis of certain drugs. Additionally, it is known to have antimicrobial and antifungal properties, making it useful in various personal care and healthcare products. Overall, 4-Benzyloxy-1,3-butanediol is a versatile chemical with diverse applications in various industries.

InChI:InChI=1/C11H16O3/c12-7-6-11(13)9-14-8-10-4-2-1-3-5-10/h1-5,11-13H,6-9H2

Upstream product

• 3068-00-6 D,L-1,2,4-butanetriol 
• 636-61-3 D-Malic acid 
• 2930-05-4 Benzyloxymethyl-oxiran 
• 78513-15-2 <2R-(2β,3α)>-3-<(phenylmethoxy)methyl>oxiranemethanol 
• 69152-88-1 4-(benzyloxy)-2-buten-1-ol 
• 97-67-6 (S)-Malic acid 

Downstream Products

• 129201-32-7 N'-[1-(4-Benzyloxymethyl-[1,3]dioxan-2-yl)-meth-(E)-ylidene]-N,N-dimethyl-hydrazine 
• 1115323-56-2 4-(benzyloxymethyl)-2,2-diphenyl-1,3-dioxane 
• 129201-37-2 N'-[1-(4-Benzyloxymethyl-[1,3]dioxan-2-yl)-pentyl]-N,N-dimethyl-hydrazine 
• 875614-83-8 (E)-ethyl 6-(benzyloxy)-5-hydroxyhex-2-enoate 
• 949932-76-7 (S)-1-(benzyloxy)-4-(tert-butyldimethylsilyloxy)butan-2-ol 

Relevant articles and documents

Copper-catalyzed cross-coupling reactions of epoxides with gem-diborylmethane: access to γ-hydroxyl boronic esters

Herein, we describe a novel copper-catalyzed epoxide opening reaction with gem-diborylmethane. Aliphatic, aromatic epoxides as well as aziridines are converted to the corresponding γ-pinacolboronate alcohols or amines in moderate to excellent yields. This new reaction provides beneficial applications for classic epoxide substrates as well as interesting gem-diborylalkane reagents.

Studies toward the synthesis of iejimalides A-D: Preparation of the C3-11 and C12-C24 fragments

The convergent synthesis of the C3-C11 and C12-C24 fragments of the iejimalides A-D is described. The C3-C11 fragment is obtained by a cross-metathesis reaction, while the C12-C24 fragment is derived from a Still-Gennari modified Horner-Wadsworth-Emmons o

A Facile and Highly Stereoselective Synthesis of (R)- and (S)-oxirane

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