5-Bromovaleronitrile

  • Name: 5-Bromovaleronitrile
  • CAS: 5414-21-1
  • Purity: 99%
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Factory Sells Best Quality 5-Bromovaleronitrile 5414-21-1 with USP

  • Molecular Formula: C5H8BrN
  • Molecular Weight: 162.029
  • Appearance/Colour: CLEAR COLOURLESS TO LIGHT YELLOW LIQUID 
  • Vapor Pressure: 0.037mmHg at 25°C 
  • Refractive Index: n20/D 1.478(lit.)  
  • Boiling Point: 240.9 °C at 760 mmHg 
  • Flash Point: 99.5 °C 
  • PSA： 23.79000 
  • Density: 1.377 g/cm3 
  • LogP: 2.07518 

5-Bromovaleronitrile(Cas 5414-21-1) Usage

InChI:InChI=1/C5H8BrN/c6-4-2-1-3-5-7/h1-4H2

5414-21-1 Relevant articles

Synthetic Studies on d-Biotin, Part 6:1 An Expeditious and Enantiocontrolled Approach to the Total Synthesis of d-Biotin via a Polymer-Supported Chiral Oxazaborolidine-Catalyzed Reduction of meso-Cyclic Imide Strategy

Chen, Fen-Er,Yuan, Jian-Li,Dai, Hui-Fang,Kuang, Yun-Yan,Chu, Yong

, p. 2155 - 2160 (2007/10/03)

An efficient and highly enantioselective...

Synthesis of pyridine-containing macrocycles by cobalt-mediated trimerization of triply-bonded species

Moretto,Zhang,Maryanoff

, p. 3157 - 3158 (2007/10/03)

-

Cortamidine oxide, a novel disulfide metabolite from the New Zealand basidiomycete (mushroom) cortinarius species

Nicholas,Blunt,Munro

, p. 341 - 344 (2007/10/03)

Three disulfide metabolites were isolate...

Orthocarbonsaeure-ester mit 2,4,10-Trioxaadamantanstruktur als Carboxylschutzgruppe; Verwendung zur Synthese von substituierten Carbonsaeuren mit Hilfe von Grignard-Reagenzien

Voss, Gundula,Gerlach, Hans

, p. 2294 - 2307 (2007/10/02)

The surprising stability of 2,4,10-triox...

5414-21-1 Process route

1,4-dibromo-butane
110-52-1

1,4-dibromo-butane

potassium cyanide
151-50-8

potassium cyanide

5-bromopentan-1-nitrile
5414-21-1

5-bromopentan-1-nitrile

Conditions
Conditions Yield
With 18-crown-6 ether; In acetonitrile; for 16h; Heating;
78%
With methanol;
With ethanol;
In ethanol; water; Heating;
1,4-dibromo-butane
110-52-1

1,4-dibromo-butane

sodium cyanide
143-33-9,25596-52-5

sodium cyanide

5-bromopentan-1-nitrile
5414-21-1

5-bromopentan-1-nitrile

Conditions
Conditions Yield
In N,N-dimethyl-formamide; at 35 ℃; for 2h;
80%
In dimethyl sulfoxide; at 60 - 70 ℃; for 0.5h;
38%
In dimethyl sulfoxide; at 60 ℃; for 1h;
55 % Turnov.

5414-21-1 Upstream products

  • 110-52-1
    110-52-1

    1,4-dibromo-butane

  • 151-50-8
    151-50-8

    potassium cyanide

  • 61862-52-0
    61862-52-0

    5-hydroxy pentanal oxime

  • 143-33-9
    143-33-9

    sodium cyanide

5414-21-1 Downstream products

  • 5454-83-1
    5454-83-1

    5-bromovaleric acid methyl ester

  • 101260-30-4
    101260-30-4

    5-[4-(2-chloro-phenyl)-piperazino]-pentylamine

  • 14660-52-7
    14660-52-7

    ethyl 5-bromovalerate

  • 59121-25-4
    59121-25-4

    5-(methylsulfanyl)pentanenitrile

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