Welcome to LookChem.com Sign In|Join Free
  • or
2,4-bis(diethoxycarbonylmethylene)-1,3-dithietane is a complex organic compound characterized by a 1,3-dithietane core, which consists of two sulfur atoms connected to a central carbon atom, forming a three-membered ring. The compound is further distinguished by two diethoxycarbonylmethylene groups attached to the carbon atoms at positions 2 and 4. These groups are esters derived from diethyl oxalate, where the hydroxyl groups are replaced by ethoxy groups. The compound is of interest in organic chemistry, particularly in the synthesis of sulfur-containing compounds and as a precursor in the preparation of various chemical intermediates. It is known for its potential applications in the development of pharmaceuticals and other specialty chemicals, although its use is typically limited to research settings due to its reactivity and the complexity of its synthesis.

7555-16-0

Post Buying Request

7555-16-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7555-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7555-16-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,5 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7555-16:
(6*7)+(5*5)+(4*5)+(3*5)+(2*1)+(1*6)=110
110 % 10 = 0
So 7555-16-0 is a valid CAS Registry Number.

7555-16-0Relevant academic research and scientific papers

EFECT OF SUBSTITUENTS AND REACTION CONDITIONS ON THE DICHOTOMY OF THE REACTION OF 1,1-ETHENEDITHIOLATES WITH ACTIVATED HALOGENOACETYLENES AND Β,Β-DIHALOGENOVINYL DERIVATIVES

Komarova, E. N.,Dmitriev, L. B.,Drozd, V. N.

, p. 1811 - 1818 (2007/10/02)

The effect of substituents and reaction conditions (solvents) on the dichotomy in the reaction of 1,1-ethenedithiolates with activated halogenoacetylenes and β,β-dihalogenovinyl derivatives was investigated.The reaction results in the formation of 2-alkylidene-1,3-dithioles and/or unsymmetrical 2,4-dialkylidene-1,3-dithietanes (desaurins).The second direction of the reaction could only be realized in the case of 1-acyl-2-halogenoacetylenes (1-benzoyl-2-bromoacetylene) and β,β-dichlorovinyl ketones in sufficiently polar solvents.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 7555-16-0