3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone

Base Information

Chemical Name:3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone
CAS No.:27241-66-3
Molecular Formula:C₁₃H₉Br₂NO₃S
Molecular Weight:419.093
Hs Code.:

Synonyms:3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone

Suppliers and Price of 3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone

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Technology Process of 3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone

There total 4 articles about 3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 135950-59-3,6028-97-3
3-(4-nitrophenyl)-1-(thiophen-2-yl)prop-2-en-1-one

: 27241-66-3
3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone

Guidance literature:: With bromine; In chloroform;
DOI:10.1016/j.molstruc.2015.02.069

Reference yield:

: 88-15-3,97511-16-5
2-Acetylthiophene

: 27241-66-3
3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol

2: bromine / chloroform

With bromine; sodium hydroxide; In ethanol; chloroform; 1: |Claisen-Schmidt Condensation;
DOI:10.1016/j.molstruc.2015.02.069

Reference yield:

: 555-16-8
4-nitrobenzaldehdye

: 27241-66-3
3-(p-nitrophenyl)-1-thienyl-2,3-dibromopropenone

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol

2: bromine / chloroform

With bromine; sodium hydroxide; In ethanol; chloroform; 1: |Claisen-Schmidt Condensation;
DOI:10.1016/j.molstruc.2015.02.069