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3-Benzyloxy-1,2-propanediol

  • CasNo:4799-67-1

Product Description

Factory Sells Best Quality 3-Benzyloxy-1,2-propanediol 4799-67-1 with GMP standards

  • Molecular Formula: C10H14O3
  • Molecular Weight: 182.219
  • Vapor Pressure: 1.17E-05mmHg at 25°C 
  • Melting Point: 62.7-63.4 °C 
  • Refractive Index: n20/D 1.533  
  • Boiling Point: 355.1 °C at 760 mmHg 
  • PKA: 13.65±0.20(Predicted) 
  • Flash Point: 168.6 °C 
  • PSA: 49.69000 
  • Density: 1.16 g/cm3 
  • LogP: 0.55640 

3-Benzyloxy-1,2-propanediol(Cas 4799-67-1) Usage

General Description

(±)-3-Benzyloxy-1,2-propanediol undergoes enantioseparation by ligand exchange micellar electrokinetic chromatography using borate anion as a central ion.

InChI:InChI=1/C10H14O3/c11-6-10(12)8-13-7-9-4-2-1-3-5-9/h1-5,10-12H,6-8H2

4799-67-1 Relevant articles

Dendritic Oligoglycerol Regioisomer Mixtures and Their Utility for Membrane Protein Research

Urner, Leonhard H.,Goltsche, Katharina,Selent, Marleen,Liko, Idlir,Schweder, Marc-Philip,Robinson, Carol V.,Pagel, Kevin,Haag, Rainer

, p. 2537 - 2542 (2020/12/30)

Dendrons are an important class of macro...

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 o...

Selective monochlorination of unsymmetrical vicinal diols with chlorinated iminium chlorides

Li, Chengyang,Li, Xiaotong,Wang, Yu,Wu, Xiaoyu,Xie, Xiaomin,Yang, Liqun,Zhang, Zhaoguo

supporting information, (2020/03/23)

Chlorinated iminium chlorides have been ...

POLY(PHOSPHOESTERS) FOR DELIVERY OF NUCLEIC ACIDS

-

, (2020/09/15)

Disclosed are polymers comprising the mo...

4799-67-1 Process route

Benzyloxymethyl-oxiran
2930-05-4

Benzyloxymethyl-oxiran

3-benzyloxypropan-1,2-diol
13071-59-5,17325-85-8,56552-80-8,4799-67-1

3-benzyloxypropan-1,2-diol

Conditions
Conditions Yield
With sulfuric acid; In water; at 20 ℃; for 5h;
96%
With perchloric acid; water; at 80 ℃;
90%
With perchloric acid; In water; at 80 ℃;
90%
With perchloric acid; In diethyl ether; at 20 ℃;
77%
With water; iodine; In acetonitrile; for 3h; Heating;
63%
With potassium hydroxide; In dimethyl sulfoxide; at 100 ℃;
46%
sulfuric acid; In water; acetone; for 3h; Yield given; Heating;
With base or acid;
With perchloric acid; In water; at 80 ℃; for 12h;
With perchloric acid; In water; benzene;
264 g (90%)
With sulfuric acid; at 20 ℃; for 5h;
Multi-step reaction with 2 steps
1: lithium tert-butoxide; copper(l) iodide / tetrahydrofuran / 20 h / 60 °C / Schlenk technique; Inert atmosphere
2: sodium hydroxide; dihydrogen peroxide / tetrahydrofuran / 10 h / 0 - 20 °C / Schlenk technique; Inert atmosphere
With copper(l) iodide; dihydrogen peroxide; sodium hydroxide; lithium tert-butoxide; In tetrahydrofuran;
With water; at 25 ℃; pH=7.2; enantioselective reaction; Microbiological reaction; Enzymatic reaction;
benzyl bromide
100-39-0

benzyl bromide

(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol
100-79-8,36543-79-0

(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol

3-benzyloxypropan-1,2-diol
13071-59-5,17325-85-8,56552-80-8,4799-67-1

3-benzyloxypropan-1,2-diol

Conditions
Conditions Yield
(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol; With sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil; at 0 ℃;
benzyl bromide; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil; at 0 - 20 ℃; for 3h;
With acetic acid; In water; at 20 ℃; for 24h;
97%
(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol; With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 0.166667h;
benzyl bromide; In N,N-dimethyl-formamide; for 5h;
77%
(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol; With sodium hydride; In tetrahydrofuran; at 0 - 20 ℃; for 0.5h; Inert atmosphere; Schlenk technique;
benzyl bromide; In tetrahydrofuran; Inert atmosphere; Schlenk technique;
60%

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    4-(benzyloxymethyl)-2,2-dimethyl-1,3-dioxolane

  • 100-44-7
    100-44-7

    benzyl chloride

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    (+/-)-1-benzyloxy-2,3-bis-methanesulfonyloxy-propane

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