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1,5-dihydro-benzo[e][1,2,3]trithiepine is a heterocyclic compound characterized by a benzene ring fused with a trithiepine ring system. This unique structure consists of a benzene ring with a trithiepine ring attached at the 1,5 positions, creating a seven-membered ring containing three sulfur atoms. The compound exhibits interesting chemical properties due to the presence of sulfur atoms in the ring, which can participate in various reactions and form different types of chemical bonds. Its potential applications may include pharmaceuticals, agrochemicals, and materials science, where its unique structure and reactivity could be exploited for specific purposes. However, further research and characterization are needed to fully understand its properties and potential uses.

3354-86-7

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3354-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3354-86-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3354-86:
(6*3)+(5*3)+(4*5)+(3*4)+(2*8)+(1*6)=87
87 % 10 = 7
So 3354-86-7 is a valid CAS Registry Number.

3354-86-7Relevant academic research and scientific papers

Synthesis of Cyclic Polysulfides. Reactions of Dithiols and Related Compounds with Elemental Sulfur in Liquid Ammonia

Sato, Ryu,Saito, Satoru,Chiba, Hiroshi,Goto, Takehiko,Saito, Minoru

, p. 1647 - 1652 (1988)

Many cyclic polysulfides, i.e., benzopentathiepins (3a-d), 6H-1,2,3,4,5-benzopentathiocin, 5H-1,2,3,4-benzotetrathiepin, 3H-1,2-benzodithiole, 1,5-dihydro-2,3,4-benzotrithiepin, 1,4-dihydro-2,3-benzodithiin, naphtho-1,2-dithiole, 1,2,3-trithiane, 1,2-dithiane, 2,3,4,5-tetrathiabicyclodecane, and 2,3,4,5,6-pentathiabicycloundecane, were synthesized in high yields by new reactions of their corresponding dithiols and related compounds, 1,3-benzodithiole-2-thiones (5) and 1,3-dithiolane-2-thione, with elemental sulfur in liquid ammonia at ambient temperature.In the synthesis of 3a-d from 1,2-benzenedithiol or 5, considerable increase in the product yield was observed upon adding 1,3-dinitrobenzene to the solvent used in work-up.

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