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1-(3,4-dichlorophenyl)-4-[(ethylsulfanyl)methyl]non-1-en-3-one, also known as DCMEN, is a chemical compound utilized in the realm of organic synthesis. It is characterized by its non-enolizable β-diketone structure, which includes a chlorophenyl and an ethylsulfanyl group. DCMEN is a yellow solid that exhibits solubility in organic solvents such as ethanol and acetone. Its versatile structure enables it to engage in a range of synthetic transformations, making it a valuable component in the creation of heterocyclic compounds and other biologically active molecules. However, due to its potentially hazardous nature, DCMEN requires careful handling and adherence to proper safety protocols.

74975-61-4

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74975-61-4 Usage

Uses

Used in Organic Synthesis:
DCMEN is used as a reagent in the field of organic synthesis for its ability to participate in various chemical reactions. Its unique structure allows it to be a key component in the formation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DCMEN is used as a key precursor for the synthesis of heterocyclic compounds, which are essential in the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
DCMEN is also utilized in chemical research as a model compound to study the properties and reactivity of β-diketone systems, contributing to the advancement of knowledge in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 74975-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,7 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74975-61:
(7*7)+(6*4)+(5*9)+(4*7)+(3*5)+(2*6)+(1*1)=174
174 % 10 = 4
So 74975-61-4 is a valid CAS Registry Number.

74975-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-(3,4-dichlorophenyl)-4-(ethylsulfanylmethyl)non-1-en-3-one

1.2 Other means of identification

Product number -
Other names 1-Nonen-3-one,4-dichlorophenyl)-4-[(ethylthio)methyl]-,(E)

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:74975-61-4 SDS

74975-61-4Downstream Products

74975-61-4Relevant academic research and scientific papers

The reaction of some nuclear substituted acyclic conjugated styryl ketones and related Mannich bases with ethanethiol.

Dimmock, J.R.,Smith, L.M.,Smith, P.J.

, p. 984 - 991 (2007/10/02)

The second order rate constants for the reaction of ethanethiol with a number of conjugated nuclear-substituted styryl ketones and related Mannich bases in 50percent aqueous acetonitrile was undertaken.Variation of the alkyl group adjacent to the carbonyl

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