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1-(3,4-dichlorophenyl)-4-methylidenenon-1-en-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59512-46-8

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59512-46-8 Usage

Appearance

Yellow crystalline solid

Usage

Organic synthesis and research

Classification

Chalcone derivative

Pharmacological activities

Potential anti-inflammatory, antioxidant, and anticancer properties

Structural feature

Presence of 3,4-dichlorophenyl group

Interaction with biological targets

Suggests potential lead compound for novel pharmaceuticals

Further research needed

To fully understand biological activities and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 59512-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,1 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59512-46:
(7*5)+(6*9)+(5*5)+(4*1)+(3*2)+(2*4)+(1*6)=138
138 % 10 = 8
So 59512-46-8 is a valid CAS Registry Number.

59512-46-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 1-(3,4-dichlorophenyl)-4-methylene-1-nonen-3-one

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:59512-46-8 SDS

59512-46-8Downstream Products

59512-46-8Relevant 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

Evaluation of Mannich bases and related compounds as inhibitors of mitochondrial function in yeast and inhibition of blood platelet aggregation, blood clotting, and in vitro metabolism of 5 dimethylamino 1 phenyl 1 penten 3 one hydrochloride

Dimmock,Hamon,Hindmarsh,Mills,Negrave,Rank,Robertson

, p. 482 - 488 (2007/10/06)

5 Dimethylamino 1 phenyl 1 penten 3 one hydrochloride (Ia) and 32 analogs were tested for inhibition of respiratory dependent growth in Saccharomyces cerevisiae. 13 Of the 33 compounds tested appeared to affect mitochondrial function, since the inhibition

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