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5,6-Dihydro-4H-1,3-dithiin-2-thione is a sulfur-containing heterocyclic compound with the molecular formula C3H4S3. It features a dihydro-1,3-dithiin core structure, which consists of a six-membered ring with two sulfur atoms and four carbon atoms. The compound has a thione functional group at the 2-position, which is a sulfur analog of a ketone. This chemical is known for its unique electronic properties and can be used in the synthesis of various sulfur-containing compounds. Due to its reactivity and potential applications in organic chemistry, it is an interesting molecule for researchers studying the properties and reactions of sulfur-containing heterocycles.

1748-15-8

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1748-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1748-15-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1748-15:
(6*1)+(5*7)+(4*4)+(3*8)+(2*1)+(1*5)=88
88 % 10 = 8
So 1748-15-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H6S3/c5-4-6-2-1-3-7-4/h1-3H2

1748-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dithiane-2-thione

1.2 Other means of identification

Product number -
Other names 1,cyclic carbonotrithioate

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:1748-15-8 SDS

1748-15-8Relevant academic research and scientific papers

1,3-dithian-2-ylidene and thiazolidin-2-ylidene derivatives as a novel class of antimycotic agents

Ram, Vishnu J.,Nath, Mahendra,Shukla

, p. 2137 - 2140 (1997)

Several 1,3-dithian-2-ylidens (2a-e,3), (4-methyl-1,3-dithiol-2-ylidene)(imidazol-l-yl) acetonitrile (4) and thiazolidin-2-ylidene derivatives (5a-d) were synthesized and evaluated for in vitro antifungal activity.

An Inadvertent Synthesis of Cyclic and Acyclic Trithiocarbonates under Phase-transfer Conditions

Ram, Vishnu J.,Singh, Sunil K.,Nath, Mahendra,Srivastava, Pratibha

, p. 64 - 65 (2007/10/03)

The formation of trithiocarbonates (7, 8) and ketene dithioacetals (4) from (imidazol-1-yl)acetonitrile (1a) and ethyl(imidazol-1-yl)acetate (1b) under both normal and phase-transfer conditions is delineated.

Convenient Synthesis of Alkanediyl Bis(alkyl trithiocarbonate)s from Alkanedithiols with Alkyl Halides and Carbon Disulfide in the Presence of Phase Transfer Catalyst

Sugawara, Akira,Hasegawa, Ken,Suzuki, Ken-ichi,Takahashi, Yukio,Sato, Ryu

, p. 435 - 437 (2007/10/02)

Alkanediyl bis(alkyl trithiocarbonate)s were conveniently synthesized by treating alkanedithiols with alkyl halides and carbon disulfide in the presence of a phase transfer catalyst.

GENERATION OF 1,2-ETHANEBIS(TRITHIOCARBONIC ACID) DIANION FROM 2,2'-BIS-1,3-DITHIOLANE AND ITS REACTION WITH ALKYL HALIDES

Tanimoto, Shigeo,Oida, Tatuo,Hatanaka, Kouhei,Sugimoto, Toyonari

, p. 655 - 658 (2007/10/02)

Generation of 1,2-ethanbis(trithiocarbonic acid) dianion from 2,2'-bis-1,3-dithiolane and its reaction with alkyl halides were investigated.

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