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1-(diphenylphosphorothioyl)piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35259-94-0

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35259-94-0 Usage

Type of compound

Phosphorothioate

Structural feature

Contains a piperidine ring

Common use

Organophosphorus pesticide

Toxicity

Known for its toxicity

Health and environmental impact

Widely studied for potential harmful effects on human health and the environment

Classification

Cholinesterase inhibitor

Mechanism of action

Inhibits the enzyme responsible for breaking down acetylcholine, a neurotransmitter

Symptoms of exposure

Nausea, dizziness, difficulty breathing, and even death in severe cases

Safety precautions

Proper handling and precautions should be taken when working with or around this chemical

Check Digit Verification of cas no

The CAS Registry Mumber 35259-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,5 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35259-94:
(7*3)+(6*5)+(5*2)+(4*5)+(3*9)+(2*9)+(1*4)=130
130 % 10 = 0
So 35259-94-0 is a valid CAS Registry Number.

35259-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenyl-piperidin-1-yl-sulfanylidene-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names diphenyl(piperidino)phosphine sulfide

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:35259-94-0 SDS

35259-94-0Relevant academic research and scientific papers

Aminolyses of aryl diphenylphosphinates and diphenylphosphinothioates: Effect of modification of electrophilic center from P=O to P=S

Um, Ik-Hwan,Akhtar, Kalsoom,Shin, Young-Hee,Han, Jeong-Yoon

, p. 3823 - 3829 (2008/02/02)

(Chemical Equation Presented) A kinetic study is reported for aminolysis of aryl diphenylphosphinothioates (2a-i). The phosphinothioates 2a-i are less reactive than aryl diphenylphosphinates (1a-i), the oxygen analogues of 2a-i, regardless of the basicity

Organic phosphorus compounds 106.1 a 31P-NMR study of phosphinous-, phosphinic-, and thiophosphinic amides

Maier, Ludwig,Diel, Peter J.

, p. 273 - 300 (2007/10/03)

The synthesis, physical, chemical and spectroscopic properties of eight different types of phosphinous-, phosphinic-and thiophosphinic amides are reported. It is shown that the 31P-chem. shifts of tertiary amides are at lower magnetic field than that of secondary amides. As an exception, in the bis(tertiary butyl) series this trend is reversed.

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