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1,4-Dithiepane is a heterocyclic compound consisting of a six-membered ring with two sulfur atoms at positions 1 and 4. It is an analog of cyclohexane, where two of the carbon atoms are replaced by sulfur atoms. This sulfur-containing compound exhibits unique chemical properties due to the presence of sulfur, which can participate in various reactions, such as oxidation and reduction. 1,4-Dithiepane is of interest in organic chemistry and has potential applications in the synthesis of pharmaceuticals and other sulfur-containing compounds. Its structure and reactivity make it a valuable building block for the development of new molecules with specific properties.

6008-55-5

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6008-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6008-55-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6008-55:
(6*6)+(5*0)+(4*0)+(3*8)+(2*5)+(1*5)=75
75 % 10 = 5
So 6008-55-5 is a valid CAS Registry Number.

6008-55-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dithiacycloheptane

1.2 Other means of identification

Product number -
Other names 1,4-Dithiacycloheptan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6008-55-5 SDS

6008-55-5Downstream Products

6008-55-5Relevant academic research and scientific papers

A novel synthesis of cyclic polythioethers using liquid-liquid phase-transfer catalysis

Takido, Toshio,Toriyama, Masaharu,Ogura, Kazuhiro,Kamijo, Haruo,Motohashi, Shigeyasu,Seno, Manabu

, p. 1295 - 1301 (2007/10/03)

The synthesis of cyclic polythioethers has been achieved by the reactions of dithiols with alkyl dihalides. Thiols are not only hard to handle owing to their unpleasant smell, but also they are easily oxidizable, thus it is not easy to obtain various dithiols. However, we have developed a procedure for the preparation cyclic polythioethers by the reaction of dithioiminium salts with alkyl dihalides using phase-transfer catalyst without the use of dithiols, and have examined the ion recognition of these compounds.

Synthetic potentialities of sulfonylsulfonium salts: A new approach to the preparation of disulfonium dications

Shevchenko,Nenaidenko,Balenkova

, p. 1415 - 1420 (2007/10/03)

A new efficient method for the generation of disulfonium dications whose subsequent hydrolysis selectively affords monosulfoxides was developed based on the oxidation of bis-sulfides by trifluoromethanesulfonic anhydride.

Formation of sulfur-centered cation radicals by photofragmentation

Glass,Broeker,Anklam,Asmus

, p. 1721 - 1724 (2007/10/02)

The selected dialkyl dithioethers 1,5-dithiocane, 1,4-dithiepane, 1,4-dithiane, and 2,6-dithiaheptane are readily monoalkylated in nitromethane by tert-butyl 0-trifluoromethanesulfonyl-3-hydroxyperoxypropanoate 6, to give the corresponding sulfonium salt peresters 2a-c, and 3 in good yield. Laser flash photolysis of these compounds affords the known two-sulfur, three-electron stabilized cation radicals 2a, b, and 5 which were characterized by optical absorption spectroscopy.

Heterocyclisation alkylante radicalaire par photolyse de sulfures ethyleniques. III. Photolyse de sulfures de butene-3 yle-1 et hexene-5 yle-1

Bastien, Gerard,Surzur, Jean-Marie

, p. 84 - 88 (2007/10/02)

Photolysis of allyl but-3-en-1-yl sulfide (I) gives the thiolan 3 and the 3-allylthiolan 4 resulting from "forbidden" 5-endotrig cyclization.Photolysis of allyl hex-5-en-1-yl sulfide (III) gives, besides the mixture of six- and seven-membered non-alkylated heterocycles 10 and 11, exclusively the alkylated 2-(but-3-enyl) thian 12.These and other results confirm and generalize the mechanism proposed earlier for the photolytic cyclization of pent-4-enyl sulfides.Photolitic cleavage of unsaturated allyl or benzyl sulfides gives the unsaturated thiyl radical.The unsaturated radical undergoes an intramolecular reversible addition out of the cage.Then the more stable cyclized radical is trapped selectively by the allyl or benzyl radical.

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