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methyl 4-pyridyl disulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96848-60-1

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96848-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96848-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96848-60:
(7*9)+(6*6)+(5*8)+(4*4)+(3*8)+(2*6)+(1*0)=191
191 % 10 = 1
So 96848-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NS2/c1-8-9-6-2-4-7-5-3-6/h2-5H,1H3

96848-60-1SDS

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 4-(methyldisulfanyl)pyridine

1.2 Other means of identification

Product number -
Other names 4-(Methyldithio)pyridine

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:96848-60-1 SDS

96848-60-1Downstream Products

96848-60-1Relevant academic research and scientific papers

Bistable Hofmann-Type FeIISpin-Crossover Two-Dimensional Polymers of 4-Alkyldisulfanylpyridine for Prospective Grafting of Monolayers on Metallic Surfaces

Turo-Cortés, Rubén,Valverde-Mu?oz, Francisco Javier,Meneses-Sánchez, Manuel,Mu?oz, M. Carmen,Bartual-Murgui, Carlos,Real, José Antonio

, p. 9040 - 9049 (2021)

Aiming at investigating the suitability of Hofmann-type two-dimensional (2D) coordination polymers {FeII(Lax)2[MII(CN)4]} to be processed as single monolayers and probed as spin crossover (SCO) junctions in spintronic devices, the synthesis and characterization of the MII derivatives (MII = Pd and Pt) with sulfur-rich axial ligands (Lax = 4-methyl- and 4-ethyl-disulfanylpyridine) have been conducted. The thermal dependence of the magnetic and calorimetric properties confirmed the occurrence of strong cooperative SCO behavior in the temperature interval of 100-225 K, featuring hysteresis loops 44 and 32.5 K/21 K wide for PtII-methyl and PtII/PdII-ethyl derivatives, while the PdII-methyl derivative undergoes a much less cooperative multistep SCO. Excluding PtII-methyl, the remaining compounds display light-induced excited spin-state trapping at 10 K with TLIESST temperatures in the range of 50-70 K. Single-crystal studies performed in the temperature interval 100-250 K confirmed the layered structure and the occurrence of complete transformation between the high- and low-spin states of the FeII center for the four compounds. Strong positional disorder seems to be the source of elastic frustration driving the multistep SCO observed for the PdII-methyl derivative. It is expected that the peripheral disulfanyl groups will favor anchoring and growing of the monolayer on gold substrates and optimal electron transport in the device.

Convenient Unsymmetrical Disulfane Synthesis: Basic Zeolite-Catalyzed Thiol-Disulfane Exchange Reaction

Yamamoto, Eiji,Kawai, Yasutaka,Takakura, Kei,Kimura, Moemi,Murayama, Haruno,Matsueda, Hironobu,Otsuki, Shujiro,Sakata, Hiroshi,Tokunaga, Makoto

, p. 4694 - 4699 (2021/10/14)

Convenient catalytic synthetic methods for the preparation of unsymmetrical disulfanes are described. Na-exchanged X type zeolite (Na-X), commercially available as MS-13X, effectively catalyzes thiol-disulfane exchange reactions with 1.0 equivalent of thi

SULFUR-CONTAINING COMPOUNDS AS ANTI-PROLIFERATIVE AGENTS

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Paragraph 55-56, (2013/03/26)

Novel sulphur containing compounds of the formula RSSCH3, wherein R is pyridine, phenylamine or pynmidine, and pharmaceutically acceptable salts thereof are disclosed, which have utility as anti-proliferative agents against mammalian cells. The invention provides a method for synthesizing the sulphur-containing compounds.

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