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3-(phenylsulfanyl)propanehydrazide is a chemical compound with the molecular formula C9H12N2S. It is a derivative of hydrazine, featuring a phenylsulfanyl (phenylthio) group attached to a propane backbone. 3-(phenylsulfanyl)propanehydrazide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the creation of sulfonamide-based compounds. The presence of the phenylsulfanyl group endows the molecule with unique chemical properties, such as increased lipophilicity and potential for hydrogen bonding, which can influence its reactivity and interactions with other molecules. The compound is typically synthesized through the reaction of 3-aminopropanol with phenylsulfanyl chloride or a related sulfanylating agent. Due to its reactivity, it is often used as an intermediate in the preparation of more complex molecules, highlighting its importance in organic chemistry and the pharmaceutical industry.

6292-69-9

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6292-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6292-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6292-69:
(6*6)+(5*2)+(4*9)+(3*2)+(2*6)+(1*9)=109
109 % 10 = 9
So 6292-69-9 is a valid CAS Registry Number.

6292-69-9SDS

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 3-phenylsulfanylpropanehydrazide

1.2 Other means of identification

Product number -
Other names 3-(phenylthio)propanohydrazide

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:6292-69-9 SDS

6292-69-9Downstream Products

6292-69-9Relevant academic research and scientific papers

Direct Michael addition to electron-deficient alkenes using diorganyl dichalcogenides (Te/S) and NaBH4/PEG-400

Perin, Gelson,Borges, Elton L.,Peglow, Thiago J.,Lenard?o, Eder J.

, p. 5652 - 5655 (2014)

Nucleophilic species of tellurium and sulfur were generated in situ from the reaction of the respective diorganyl dichalcogenides with NaBH4in PEG-400 as solvent and selectively added to electron-deficient alkenes. Chalcogenolate anions were directly added at mild conditions by this simple procedure and in all cases furnished the respective Michael adducts in short reaction times and good yields.

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