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3-thiocyanatopentane-2,4-dione is a chemical compound with the molecular formula C6H7NO2S. It is a derivative of pentane-2,4-dione, also known as acetylacetone, with a thiocyanate group (-SCN) attached to the third carbon atom. 3-thiocyanatopentane-2,4-dione is an organic compound that belongs to the class of thiocyanates, which are characterized by the presence of the SCN functional group. It is a colorless to pale yellow solid and is soluble in organic solvents. The compound has potential applications in the synthesis of various organic compounds and as a reagent in chemical reactions. Due to its reactivity, it should be handled with care, and its properties and uses are of interest to researchers in the field of organic chemistry.

7153-90-4

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7153-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7153-90-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7153-90:
(6*7)+(5*1)+(4*5)+(3*3)+(2*9)+(1*0)=94
94 % 10 = 4
So 7153-90-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2S/c1-4(8)6(5(2)9)10-3-7/h6H,1-2H3

7153-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dioxopentan-3-yl thiocyanate

1.2 Other means of identification

Product number -
Other names 3-thiocyanato-2,4-pentanedione

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:7153-90-4 SDS

7153-90-4Relevant academic research and scientific papers

Heteropoly acids as heterogeneous and reusable catalyst for α-thiocyanation of ketones

Chaskar, Atul C.,Yadav, Arun A.,Langi, Bhushan P.,Murugappan, Anita,Shah, Chetan

experimental part, p. 2850 - 2856 (2010/10/20)

Simple, efficient, and mild method for -thiocyanation of ketones in presence of heteropolyacid has been developed. This methodology offered -oxothiocyanates in good to excellent yields at room temperature in a highly selective manner. The catalyst could b

α-thiocyanation of carbonyl and β-dicarbonyl compounds using (dichloroiodo)benzene-lead(II) thiocyanate

Prakash,Kaur,Batra,Rani,Singh,Moriarty

, p. 2019 - 2023 (2007/10/03)

The combination reagent (dichloroiodo)benzene and lead(II) thiocyanate in dichloromethane effects oxidation of various enol silyl ethers, ketene silyl acetals, and β-dicarbonyl compounds, thereby providing an efficient and convenient method for α-thiocyanation of carbonyl and β-dicarbonyl compounds.

Pseudohalogen chemistry. XI. Some aspects of the chemistry of octhiocyanato-β-dicarbonyl compounds

Atkins, Elaine F.,Dabbs, Steven,Guy, Robert G.,Mahomed, Akbar A.,Mountford, Philip

, p. 7253 - 7264 (2007/10/02)

Enolised α-thiocyanato-β-dicarbonyl compounds dimerise in ethanol at room temperature to give tautomeric 4,5-disubstituted 2-amino- and 2-acetamido-thiazoles by a C-S-C + C-N cyclisation. Tautomerism is due to the unusual 4-(β-dicarbonyl-α-thio) substituent. Competing intramolecular cyclisations lead to minor amounts of heterocycles containing the thiazole and/or oxathiole ring systems.

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