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2495-39-8

  • Product NameSodium allylsulfonate
  • MFC3H5NaO3S
  • Molecular Weight144.127
  • Purity99%
  • Appearancesolid
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Product Details

Quick Details

  • CasNo: 2495-39-8
  • MF: C3H5NaO3S
  • Appearance: solid
  • Purity: 99%

  • Molecular Formula:C3H5NaO3S
  • Molecular Weight:144.127
  • Appearance/Colour:solid 
  • Vapor Pressure:0Pa at 25℃ 
  • Melting Point:0oC 
  • Flash Point:144.124oC 
  • PSA:65.58000 
  • Density:1.206 g/cm3 
  • LogP:0.79840 

Sodium allylsulfonate(Cas 2495-39-8) Usage

Chemical Properties

White to Almost white powder to crystal.

Uses

Sodium allyl sulfonate is used as a basic brightener in nickel electroplating baths. It is also used as pharmaceutical intermediates.

Flammability and Explosibility

Nonflammable

InChI:InChI=1/C3H6O3S/c1-2-3-7(4,5)6/h2H,1,3H2,(H,4,5,6)/p-1

2495-39-8 Relevant articles

Synthesis of sodium allyl sulfonate in an aqueous medium by micellar catalysis with methoxy polyethylene glycol methacrylates

Orekhov,Kazantsev,Sivokhin,Khokhlova

, p. 881 - 886 (2014)

Micellar catalysis with various polyoxye...

Ring closing metathesis and metal-catalyzed cyclopropanation for the preparation of sultone derivatives

Ali, Korany A.,Metz, Peter

, p. 19 - 29 (2019/04/17)

Ring closing metathesis (RCM) using Grub...

Synthesis method of sodium allysulfonate

-

Paragraph 0023-0034, (2019/02/04)

The invention discloses a synthesis meth...

Olefination with Sulfonyl Halides and Esters: E-Selective Synthesis of Alkenes from Semistabilized Carbanion Precursors

Górski, Bartosz,Basiak, Dariusz,Talko, Alicja,Basak, Tymoteusz,Mazurek, Tomasz,Barbasiewicz, Micha?

supporting information, p. 1774 - 1784 (2018/04/27)

Carbanions of sulfonyl halides and activ...

6-MEMBERED URACIL ISOSTERES

-

Paragraph 0779, (2018/06/12)

Provided herein are dUTPase inhibitors, ...

2495-39-8 Process route

4-tert-Butylcatechol
98-29-3

4-tert-Butylcatechol

sodium prop-2-ene-1-sulfonate
2495-39-8

sodium prop-2-ene-1-sulfonate

Conditions
Conditions Yield
With sodium metabisulfite; N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide; In water; at 40 - 50 ℃; under 2250.23 Torr; Temperature; Reagent/catalyst; Pressure;
98.93%
allyl bromide
106-95-6

allyl bromide

sodium prop-2-ene-1-sulfonate
2495-39-8

sodium prop-2-ene-1-sulfonate

Conditions
Conditions Yield
With sodium sulfite;
78%
With sodium sulfite; In ethanol; water; for 3h; Heating / reflux;
76%
With sodium sulfite; In ethanol; water; for 2.5h; Heating;
75%
With sodium sulfite; In water; for 24h; Reflux;
 
With sodium sulfite; In water; at 100 ℃;
 
With sodium sulfite; In water; at 100 ℃; for 16h;
 
With sodium sulfite; In water; for 8h; Reflux;
 

2495-39-8 Upstream products

  • 107-05-1
    107-05-1

    3-chloroprop-1-ene

  • 106-95-6
    106-95-6

    allyl bromide

  • 7757-83-7
    7757-83-7

    sodium sulfite

  • 98-29-3
    98-29-3

    4-tert-Butylcatechol

2495-39-8 Downstream products

  • 14418-84-9
    14418-84-9

    allylsulfonyl chloride

  • 51116-03-1
    51116-03-1

    sodium 2,3-dibromopropane-1-sulfonate

  • 189756-89-6
    189756-89-6

    2-bromopropane-1,3-sultone

  • 7783-06-4
    7783-06-4

    hydrogen sulfide

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