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74637-14-2

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74637-14-2 Usage

Uses

1,4-Dithian-2-one is a building block.

Check Digit Verification of cas no

The CAS Registry Mumber 74637-14-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,3 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74637-14:
(7*7)+(6*4)+(5*6)+(4*3)+(3*7)+(2*1)+(1*4)=142
142 % 10 = 2
So 74637-14-2 is a valid CAS Registry Number.

74637-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dithian-2-one

1.2 Other means of identification

Product number -
Other names 2-oxo-1,4-dithiacyclohexane

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:74637-14-2 SDS

74637-14-2Relevant articles and documents

Reaction of three cyclic thioester ligands with triiron dodecacarbonyl and possible reaction mechanisms

Xiao, Zhiyin,Wang, Yongli,Chen, Xueyuan,Long, Jiao,Wei, Zhenhong

, p. 1595 - 1601 (2017)

Abstract : Three cyclic thioesters of the formula “-SCH2CH2SCO(CH2)n-” (L1, n = 0 ? L2, = 1 , L3, n = 2) and their reactions with Fe 3(CO) 12 are reported. All the reactions produced a known diiron complex, [Fe 2(μ - S 2C 2H 4) (CO) 6] (1), which suggested that in the reactions, cleavage of C-S bond to generate “SCH 2CH 2S ” fragment is a common pathway for all the three ligands. In the case of ligand L2, a new complex 2, [Fe 2{ μ - SC 2H 4(SCH 2) - κ } (CO) 6] was isolated and structurally characterized. In the reaction of ligand L3, an unknown iron carbonyl product was isolated in addition to complex 1. Although its precise structure was not established due to its instability and low yield, its infrared spectrum and decomposing into complex 1 implied that the product may be a cluster with higher nuclearity. The experimental observations suggested that with the increase of the ring size of the cyclic thioester ligands, further bond cleavages were involved in the reaction in addition to that leading to complex 1. GRAPHICAL ABSTRACT: SYNOPSIS Reaction of cyclic thioester ligands with triiron dodecacarbonyl leads to scission of C-S (C) bond which is initiated by the coordination of the S atom to the Fe atom. The larger the ring size of the ligand, the more diverse are the bond cleavages. [Figure not available: see fulltext.].

Chealators of type XN1 S1 X1 for radioactive isotopes, their metal complexes and their diagnostic and therapeutical uses

-

, (2008/06/13)

This invention relates to new bifunctional chelating agents with intermittent chalcogen atoms, pharmaceuticals containing these compounds, their use in radiodiagnostics and radiotherapy, and methods for the production of these compounds. The compound according to the invention has the general formula (I) where M represents a radionuclide and L a ligand of the general formula (II). It was found, surprisingly, that these new, bifunctional chelating agents with intermittent chalcogen atoms and their coupling products with compounds that accumulate specifically are excellently suited for producing radiopharmaceuticals for diagnostic and therapeutic purposes.

A novel oxidative cleavage reaction with Pb(OAc)4 via dithioacetal derivatives

Hiroi,Sato,Matsuo

, p. 558 - 566 (2007/10/02)

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