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2,4-Dibromo-1,5-diphenyl-1,4-pentadien-3-one is a chemical compound characterized by the presence of two bromine atoms on a five-carbon chain that is flanked by two benzene rings. This yellow solid is known for its strong odor and is recognized for its applications in the synthesis of pharmaceuticals and organic compounds. It also serves as a reagent in organic chemistry, particularly for the formation of carbon-carbon and carbon-heteroatom bonds. Due to its potential for skin and eye irritation, as well as toxic effects if ingested or inhaled, it is classified as a hazardous substance that requires careful handling.

51110-61-3

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51110-61-3 Usage

Uses

Used in Pharmaceutical Synthesis:
2,4-Dibromo-1,5-diphenyl-1,4-pentadien-3-one is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new compounds with potential therapeutic properties, contributing to the development of novel medications.
Used in Organic Chemistry as a Reagent:
In the field of organic chemistry, 2,4-Dibromo-1,5-diphenyl-1,4-pentadien-3-one is utilized as a reagent for facilitating the formation of carbon-carbon and carbon-heteroatom bonds. This capability is crucial for the synthesis of complex organic molecules and contributes to the advancement of organic chemistry research and applications.
Used in Chemical Research:
2,4-Dibromo-1,5-diphenyl-1,4-pentadien-3-one is also employed in chemical research to explore its properties and potential applications. Its reactivity and structural features make it a valuable subject for studies aimed at understanding and improving synthetic methodologies and developing new chemical processes.
Used in Chemical Education:
As a representative of a class of compounds with specific reactivity, 2,4-Dibromo-1,5-diphenyl-1,4-pentadien-3-one is used in educational settings to teach students about organic synthesis, reactivity patterns, and the properties of functional groups. It serves as a practical example in lectures and laboratory exercises.

Check Digit Verification of cas no

The CAS Registry Mumber 51110-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,1 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51110-61:
(7*5)+(6*1)+(5*1)+(4*1)+(3*0)+(2*6)+(1*1)=63
63 % 10 = 3
So 51110-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H12Br2O/c18-15(11-13-7-3-1-4-8-13)17(20)16(19)12-14-9-5-2-6-10-14/h1-12H/b15-11-,16-12u

51110-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1Z,4Z)-2,4-dibromo-1,5-diphenylpenta-1,4-dien-3-one

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:51110-61-3 SDS

51110-61-3Downstream Products

51110-61-3Relevant academic research and scientific papers

A novel and one step procedure for preparation of α-bromo-α,β-unsaturated carbonyl compounds

Ramanarayanan,Shukla, Vidyanand G.,Akamanchi

, p. 2059 - 2061 (2007/10/03)

A new one step method is developed for the preparation of α-bromo-α,β-unsaturated carbonyl compounds in moderate to good yields from corresponding α,β-unsaturated carbonyl compounds using DMP [1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(IH)-one] and te

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