5197-95-5

  • Product Name:Benzyltriethylammonium bromide
  • Molecular Formula:C13H22N.Br
  • Purity:99%
  • Molecular Weight:272.228
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Product Details;

CasNo: 5197-95-5

Molecular Formula: C13H22N.Br

Appearance: white to light yellow crystal powder

Good Supplier In China Fast Delivery Benzyltriethylammonium bromide 5197-95-5 Sales promotion qualified

  • Molecular Formula:C13H22N.Br
  • Molecular Weight:272.228
  • Appearance/Colour:white to light yellow crystal powder 
  • Melting Point:193-195 °C (dec.)(lit.) 
  • Refractive Index:1.5260 (estimate) 
  • Density:1.2838 (rough estimate) 

Benzyltriethylammonium bromide(Cas 5197-95-5) Usage

Chemical Properties

white to light yellow crystal powde

InChI:InChI=1/C13H22N.BrH/c1-4-14(5-2,6-3)12-13-10-8-7-9-11-13;/h7-11H,4-6,12H2,1-3H3;1H/q+1;/p-1

5197-95-5 Relevant articles

Benzylic Ammonium Ylide Mediated Epoxidations

Roiser, Lukas,Robiette, Rapha?l,Waser, Mario

supporting information, p. 1963 - 1968 (2016/08/10)

A high yielding synthesis of stilbene ox...

Gas-phase chemistry of benzyl cations in dissociation of N-Benzylammonium and N-benzyliminium ions studied by mass spectrometry

Chai, Yunfeng,Wang, Lin,Sun, Hezhi,Guo, Cheng,Pan, Yuanjiang

experimental part, p. 823 - 833 (2012/09/07)

In this study, the fragmentation reactio...

EFFECTS OF SUBSTITUENTS IN THE BENZYL BROMIDE ON THE KINETICS OF THE BENZYLATION OF AMINES

Shpan'ko, I. V.,Korostylev, A. P.,Rusu, L. N.

, p. 1715 - 1723 (2007/10/02)

The kinetics of the reactions of 3- and ...

GEMINAL SYSTEMS. 19. REACTIONS OF AMINOMETHYLPHOSPHINES WITH ELECTROPHILIC REAGENTS

Kostyanovskii, R. G.,El'natanov, Yu. I.,Shikhaliev, Sh. M.,Ignatov, S. M.,Chervin, I. I.

, p. 1433 - 1441 (2007/10/02)

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5197-95-5 Process route

benzyl bromide
100-39-0

benzyl bromide

triethylamine
121-44-8

triethylamine

benzyltriethylammonium bromide
5197-95-5

benzyltriethylammonium bromide

Conditions
Conditions Yield
In tetrahydrofuran; ethanol; at 25 ℃; for 24h; Inert atmosphere;
98%
In 1,4-dioxane; water; at 25 ℃; Rate constant; α-deuterium isotope effect, further nucleophiles (SCN-, S2O3-);
In nitrobenzene; at 40 ℃; Rate constant; Mechanism;
at 70 ℃;
ethyl bromide
74-96-4

ethyl bromide

N,N-diethylbenzylamine
772-54-3

N,N-diethylbenzylamine

benzyltriethylammonium bromide
5197-95-5

benzyltriethylammonium bromide

Conditions
Conditions Yield
With benzene; at 100 ℃;

5197-95-5 Upstream products

  • 74-96-4
    74-96-4

    ethyl bromide

  • 772-54-3
    772-54-3

    N,N-diethylbenzylamine

  • 100-39-0
    100-39-0

    benzyl bromide

  • 121-44-8
    121-44-8

    triethylamine

5197-95-5 Downstream products

  • 772-54-3
    772-54-3

    N,N-diethylbenzylamine

  • 103-82-2
    103-82-2

    phenylacetic acid

  • 112178-91-3
    112178-91-3

    5-Benzylsulfanyl-2-thioxo-[1,3]dithiole-4-carbonitrile

  • 112178-88-8
    112178-88-8

    (6-Amino-2-thioxo-thieno[2,3-d][1,3]dithiol-5-yl)-(4-bromo-phenyl)-methanone

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