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1,3-BIS(BENZYLOXY)-2-PROPANOL is an organic compound that serves as a versatile intermediate in the synthesis of various pharmaceuticals and other organic compounds. It possesses two benzyloxy groups attached to the first and third carbon atoms of a propane backbone, which contribute to its reactivity and potential applications in chemical synthesis.

6972-79-8

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6972-79-8 Usage

Uses

Used in Pharmaceutical Synthesis:
1,3-BIS(BENZYLOXY)-2-PROPANOL is used as a key intermediate in the synthesis of 1,3-dibenzyloxyacetone, which is a precursor to various pharmaceutical compounds. Its presence in the synthesis process allows for the creation of complex organic molecules with potential therapeutic applications.
Used in Antiviral Drug Development:
1,3-BIS(BENZYLOXY)-2-PROPANOL also serves as a precursor to antiviral intermediates, playing a crucial role in the development of antiviral medications. Its involvement in the synthesis of antiviral compounds highlights its importance in the ongoing fight against viral infections and diseases.
Used in Spasmolytic and Cholinolytic Applications:
1,3-BIS(BENZYLOXY)-2-PROPANOL exhibits spasmolytic and cholinolytic activity, making it a potential candidate for use in the treatment of various conditions related to muscle spasms and the overactivity of the parasympathetic nervous system. Its ability to relax muscles and inhibit the action of acetylcholine can be beneficial in managing symptoms associated with these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 6972-79-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6972-79:
(6*6)+(5*9)+(4*7)+(3*2)+(2*7)+(1*9)=138
138 % 10 = 8
So 6972-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H20O3/c18-17(13-19-11-15-7-3-1-4-8-15)14-20-12-16-9-5-2-6-10-16/h1-10,17-18H,11-14H2

6972-79-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Bis(benzyloxy)-2-propanol

1.2 Other means of identification

Product number -
Other names 1,3-bis(phenylmethoxy)propan-2-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6972-79-8 SDS

6972-79-8Relevant academic research and scientific papers

Characterization of hydrazine derivative: Proposed decomposition mechanism and structure elucidation of decomposition compounds

Nemoto, Takayuki,Lazoura, Eliada,Nomoto, Takashi

, p. 346 - 350 (2003)

Decomposition of protected hydrazine diol (1) hemi-oxalate, a key intermediate of the potent indolocarbazole-based DNA topoisomerase I inhibitor (2), was investigated. Spectroscopic analysis revealed that the main decomposition compounds of the hydrazine

Selective catalytic oxidation of diglycerol

Wang, Huan,Vu, Nam Duc,Chen, Guo-Rong,Métay, Estelle,Duguet, Nicolas,Lemaire, Marc

supporting information, p. 1154 - 1159 (2021/02/26)

The selective oxidation of α,α-diglycerol was studied using oxygen as a clean oxidant in the presence of a palladium/neocuproine complex. After optimization of the reaction parameters, the mono-oxidation product was obtained with 93% NMR yield (up to 76% isolated yield). The product was named “diglycerose” considering that it mainly exists as a cyclic hemi-ketal form.

Synthesis and catalytic evaluation of acidic carbons in the etherification of glycerol obtained from biodiesel production

Chiosso, María E.,Casella, Mónica L.,Merlo, Andrea B.

, p. 107 - 114 (2020/10/29)

In this paper, the catalytic behaviour of carbonaceous system (Ccs) functionalized with –SO3H groups were studied in the etherification of refined (Gly) and crude glycerol (GlyC), with benzyl alcohol (BA). This Ccs was obtained by a synthetic method with low energetic cost in only 24 h. Its catalytic activity and selectivity were studied varying the catalyst percentage (2.5, 5 and 10 wt.%), the initial reactant molar ratio and temperature (between 80 and 120 °C). A very good catalytic performance was achieved (97 % conversion after 360 min of reaction), at 120 °C, Gly:BA = 3:1 and 10 wt.% of Ccs. The high activity can be attributed to high acid site density (6.4 mmol H+/g), that also allowed us to working at lower reaction temperature (100 °C) and with less catalyst concentration (2.5 wt.%), without observing significant loss in BA conversion. Monoether (ME1) was the major product of the reaction with 72 % selectivity. The material can be reused and still gives a notable conversion of BA (about 43 %) after three successive reuses. Finally, the Ccs was active and selective to the desired products in the etherification of crude glycerol (GlyC) derived of biodiesel industry. An important BA conversion (45 %) was obtained only reducing the water content of GlyC and without carrying out any other purification and/or neutralization treatment.

Virtual Screening of Acyclovir Derivatives as Potential Antiviral Agents: Design, Synthesis, and Biological Evaluation of New Acyclic Nucleoside ProTides

Derudas, Marco,Vanpouille, Christophe,Carta, Davide,Zicari, Sonia,Andrei, Graciela,Snoeck, Robert,Brancale, Andrea,Margolis, Leonid,Balzarini, Jan,McGuigan, Christopher

, p. 7876 - 7896 (2017/10/06)

Following our findings on the anti-human immunodeficiency virus (HIV) activity of acyclovir (ACV) phosphate prodrugs, we herein report the ProTide approach applied to a series of acyclic nucleosides aimed at the identification of novel and selective antiv

The role of mesoporosity and Si/Al ratio in the catalytic etherification of glycerol with benzyl alcohol using ZSM-5 zeolites

Gonzalez-Arellano, Camino,Grau-Atienza, Aida,Serrano, Elena,Romero, Antonio A.,Garcia-Martinez, Javier,Luque, Rafael

, p. 40 - 45 (2015/06/08)

A comparative study of the influence of three different acid solids as catalysts (conventional zeolites Z15c with Si/Al = 19.5 and Z40c with Si/Al = 48.2, and a hierarchical zeolite Z40c-H with Si/Al = 50.0) for the etherification of glycerol with benzyl alcohol was performed. The catalytic activity and selectivity of these zeolites was elucidated at different catalyst contents. Three different ethers (3-benzyloxy-1,2-propanediol, which is a mono-benzyl-glycerol ether (MBG) and 1,3-dibenzyloxy-2-propanol, which is a di-benzyl-glycerol ether (DBG) and dibenzyl ether (DBz) were identified as the main products. MBG was the major product of the reaction catalyzed by the microporous Z15c zeolite with low Si/Al molar ratio, whereas DBG was formed in higher yield with the use of microporous Z40c and hierarchical Z40c-H zeolites, both of them having a similar high Si/Al molar ratio (≈50 MBG is a value-added product andit is obtained with good yield and selectivity when using the conventional zeolite Z15c as a catalyst.Under the best conditions tested, i.e., 25 mg of catalyst for 8 h at 120°C, a 62% of conversion was obtainedwithout the need of solvent, with an excellent 84% selectivity toward the MBG and no formation of DBz.

Glycerol etherification with benzyl alcohol over sulfated zirconia catalysts

Jaworski, María A.,Rodríguez Vega, Sergio,Siri, Guillermo J.,Casella, Mónica L.,Romero Salvador, Arturo,Santos López, Aurora

, p. 36 - 43 (2015/09/01)

Glycerol (GLY) etherification with benzyl alcohol (BA) was conducted with different zirconia-based heterogeneous acid catalysts, aiming to produce mono- (ME) and dibenzyl glycerol ethers (DE). Physicochemical properties of the prepared catalysts were obtained through XRD, SEM and adsorption of ammonia. The catalytic tests were performed at different temperatures (120-140°C) and initial reactant mass ratios (GLY:BA 1:1 and 2:1). The highest BA conversions were obtained with the catalyst having the highest sulfuric acid content (2S/ZrO2). An increase in the reaction temperature and the GLY:BA initial mass ratio led to an increase in the BA conversion. Two kinetic models (a potential and a hyperbolic approach) were proposed to describe the process performance, including not only reactants evolution with time, but also that of ME, DE and the undesired self-condensation product of BA (benzyl ether, BE). Kinetic parameters for each model were estimated by data fitting and both models were able to accurately describe the evolution of the system, in terms of reactants and product distribution as a function of time under the experimental conditions studied.

PROCESS FOR PREPARING PURINE DERIVATIVE

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Page/Page column 6, (2010/06/16)

A process for the preparation of famciclovir a compound of Formula (I) and its intermediates.

New drug delivery nanosystem combining liposomal and dendrimeric technology (liposomal locked-in dendrimers) for cancer therapy

Gardikis, Konstantinos,Hatziantoniou, Sophia,Bucos, Madalina,Fessas, Dimitrios,Signorelli, Marco,Felekis, Theodoros,Zervou, Maria,Screttas, Constantinos G.,Steele, Barry R.,Ionov, Maksim,Micha-Screttas, Maria,Klajnert, Barbara,Bryszewska, Maria,Demetzos, Costas

scheme or table, p. 3561 - 3571 (2011/04/26)

Liposomal locked-in dendrimers (LLDs), the combination of liposomes and dendrimers in one formulation, represents a relatively new term in the drug carrier technology. LLDs undergone appropriate physicochemical investigation can merge the benefits of lipo

Direct selective and controlled protection of multiple hydroxyl groups in polyols via iterative regeneration of stannylene acetals

Simas, Alessandro B.C.,da Silva, Angelo A.T.,dos Santos Filho, Tarcizio J.,Barroso, Pedro T.W.

supporting information; experimental part, p. 2744 - 2746 (2009/09/25)

A direct selective protection (O-benzylation) of two or more hydroxyl groups in polyols displaying diverse structural patterns was made possible by the establishment of conditions that enable an efficient turnover for the Bu2Sn group, initially

AN IMPROVED PROCESS FOR PREPARING PURINE DERIVATIVE

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Page/Page column 11, (2009/01/23)

A process for the preparation of famciclovir a compound of Formula (I) and its intermediates.

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