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18871-66-4

  • Product Name1,1-Dimethoxy-N,N-dimethylethylamine
  • Molecular FormulaC6H15NO2
  • Molecular Weight133.191
  • Purity99%
  • Appearancecoloress to pale yellow liquid
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Product Details

Quick Details

  • CasNo： 18871-66-4
  • Molecular Formula： C6H15NO2
  • Appearance： coloress to pale yellow liquid
  • Purity： 99%

Reputable Factory Supply Top Purity 99% 1,1-Dimethoxy-N,N-dimethylethylamine 18871-66-4 with Reasonable Price

  • Molecular Formula:C6H15NO2
  • Molecular Weight:133.191
  • Appearance/Colour:coloress to pale yellow liquid 
  • Vapor Pressure:19.3mmHg at 25°C 
  • Refractive Index:n20/D 1.411(lit.)  
  • Boiling Point:115.133 °C at 760 mmHg 
  • PKA:5.08±0.50(Predicted) 
  • Flash Point:8.333 °C 
  • PSA：21.70000 
  • Density:0.902 g/cm3 
  • LogP:0.51450 

1,1-Dimethoxy-N,N-dimethylethylamine(Cas 18871-66-4) Usage

Chemical Properties

clear yellow to brown liquid

Uses

N,N-Dimethylacetamide dimethyl acetal has been used as:one carbon inserting synthon in preparation of pyrimido[1,2-a][1,3,5]triazin-6-onesreagent for the synthesis of amides, diacylamines and heterocycles

General Description

Claisen type reaction of N,N-dimethylacetamide dimethyl acetal using optically active trans-3-penten-2-ol as substrate has been investigated.

InChI:InChI=1/C6H15NO2/c1-6(8-4,9-5)7(2)3/h1-5H3/p+1

18871-66-4 Relevant articles

Design, synthesis and anti-tumoractivity of novel amidine derivatives of doxifluridine

Feng, Ji Lu,Sun, Hai Ling,Geng, Dong Ping,Li, Ke

, p. 163 - 166 (2010)

A series of novel amidine derivatives of...

Degradation of cellulosic materials by heating in DMAc/LiCl

Potthast, Antje,Rosenau, Thomas,Sixta, Herbert,Kosma, Paul

, p. 7757 - 7759 (2002)

N,N-Dimethylacetamide (DMAc, 1)/lithium ...

Novel and efficient one-pot synthesis of N'-alkyl-N,N-dimethylacetamidines

Li, Zhe-Qi,Wang, Hui-Long

, p. 119 - 120 (2011)

An efficient method for the synthesis of...

Convenient Preparation of N,N-Dimethylacetamide Dimethyl Acetal

Salomon, Robert G.,Raychaudhuri, Swadesh R.

, p. 3659 - 3660 (1984)

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HETEROCYCLIC INDOLE DERIVATIVES AND MONO- OR DIAZAINDOLE DERIVATIVES

-

, (2008/06/13)

Indole derivatives and mono- or diazaind...

18871-66-4 Process route

methanol
67-56-1

methanol

(1-Methoxy-1-phenylphosphanyl-ethyl)-dimethyl-amine
89865-20-3

(1-Methoxy-1-phenylphosphanyl-ethyl)-dimethyl-amine

N,N-dimethylacetamide dimethyl acetal
18871-66-4

N,N-dimethylacetamide dimethyl acetal

phenylphosphane
638-21-1

phenylphosphane

Conditions
Conditions Yield
In acetonitrile;
 
methanol
67-56-1

methanol

N,N-dimethylamino-P-phenyl-C-methylmethylenephosphine
75589-83-2

N,N-dimethylamino-P-phenyl-C-methylmethylenephosphine

N,N-dimethylacetamide dimethyl acetal
18871-66-4

N,N-dimethylacetamide dimethyl acetal

(1-Methoxy-1-phenylphosphanyl-ethyl)-dimethyl-amine
89865-20-3

(1-Methoxy-1-phenylphosphanyl-ethyl)-dimethyl-amine

phenylphosphane
638-21-1

phenylphosphane

Conditions
Conditions Yield
In acetonitrile; Heating;
 

18871-66-4 Upstream products

  • 67-56-1
    67-56-1

    methanol

  • 75589-83-2
    75589-83-2

    N,N-dimethylamino-P-phenyl-C-methylmethylenephosphine

  • 89865-20-3
    89865-20-3

    (1-Methoxy-1-phenylphosphanyl-ethyl)-dimethyl-amine

  • 124-41-4
    124-41-4

    sodium methylate

18871-66-4 Downstream products

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    52512-61-5

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    2-(3,6-Dimethoxy-2-methyl-phenyl)-N,N-dimethyl-acetamide

;

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