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diethyl 2-(benzylthio)propane-1,3-dioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16601-28-8

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16601-28-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16601-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,0 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16601-28:
(7*1)+(6*6)+(5*6)+(4*0)+(3*1)+(2*2)+(1*8)=88
88 % 10 = 8
So 16601-28-8 is a valid CAS Registry Number.

16601-28-8Relevant academic research and scientific papers

SYNTHESES OF 2-MERCAPTO- AND 2-ALKYLTHIO-1,3-PROPANEDIOL DERIVATIVES

Aveta, Raffaele,Brandt, Alberto,Corsi, G. Bruno,Costanza, Angela Mitidieri

, p. 649 - 652 (2007/10/02)

Some synthetic routes to 2-alkylthio-1,3-propanediol derivatives, starting from commercially available compounds, are discussed.Treatment of diethyl 2-chloromalonate with thiolate anions followed by LiAlH4 reduction gave 9a,b,c in nearly 30percent overall

Synthesis of Unsymmetrical Functionalised Organic Sulphides

Singh, Harjit,Batra, Manohar S.,Singh, Paramjit

, p. 131 - 136 (2007/10/02)

Acyclic thioiminium salts and the condensed thiazolium salts in the presence of aqueous sodium hydroxide as such or under base catalyzed phase transfer catalysis conditions react with appropiate organic halides to provide corresponding unsymmetrical functionalized organic sulphides.With aqueous sodium hydroxide, thioiminium salts provide the disulphides corresponding to incipient thiol.

Synthesis of Unsymmetrical Thioethers Using Solid-Liquid Phase-transfer Catalysis

Singh, Paramjit,Batra, Manohar S.,Singh, Harjit

, p. 484 (2007/10/02)

The title compounds have been synthesised from appropriate organic halides and thioimminium salts (1) in moderate to good yields under solid-liquid phase-transfer catalysis using Triethylbenzylammonium chloride (TEBA) as a catalyst, solid KOH as a base in chloroform.

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