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3475-39-6

  • Product Name1,1,3-Tribromoacetone
  • Molecular FormulaC3H3Br3O
  • Purity99%
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Product Details

Quick Details

  • CasNo: 3475-39-6
  • Molecular Formula: C3H3Br3O
  • Purity: 99%

Factory Supply High Quality 1,1,3-Tribromoacetone 3475-39-6

3475-39-6 Name

Name

1,1,3-Tribromoacetone

Synonym

1,1,3-TribromoAceton;2-Propanone,1,1,3-tribromo-;1,1,3-tribromoacetone;1,1,3-Tribromopropan-2-one;JACS-3475-39-6;TIANFU-CHEM--1,1,3-Tribromoacetone  

3475-39-6 Chemical & Physical Properties

Boiling point

266.2±25.0 °C at 760 mmHg

Density

2.6±0.1 g/cm3

Molecular Formula

C3H3Br3O

Molecular Weight

294.767

Flash Point

115.1±9.7 °C

PSA

17.07000

LogP

3.25

Exact Mass

291.773376

Vapour Pressure

0.0±0.5 mmHg at 25°C

Index of Refraction

1.595

1,1,3-Tribromoacetone 3475-39-6 Usage

1,1,3-Tribromoacetone is a chemical compound that has been studied in various scholarly articles for its potential applications. One of its primary uses is as a reagent in organic synthesis. It can be used as a starting material for the synthesis of various compounds, such as halogenated ketones and aldehydes.

InChI:InChI=1/C3H3Br3O/c4-1-2(7)3(5)6/h3H,1H2

3475-39-6 Relevant articles

A Desymmetrization-Based Total Synthesis of Reserpine

Park, Jisook,Chen, David Y.-K.

supporting information, p. 16152 - 16156 (2018/11/23)

Reported herein is a desymmetrization-based synthetic approach to the fused polycyclic indole alkaloid reserpine. The centerpiece of the developed strategy features an internal desymmetrization process that enabled the use of a readily accessible and nonstereogenic reserpine E-ring precursor, in contrast to the synthesis-intensive and stereodefined E-ring intermediates employed in all past reserpine syntheses. Utilization of inexpensive reagents through an orchestrated sequence of carefully selected chemical transformations further highlight the overall effectiveness of the developed pathway.

A new and efficient method for the synthesis of α,α- dihaloketones by oxyhalogenation of alkynes using oxone-KX (X = Cl, Br, or I)

Madabhushi, Sridhar,Jillella, Raveendra,Mallu, Kishore Kumar Reddy,Godala, Kondal Reddy,Vangipuram, Venkata Sairam

supporting information, p. 3993 - 3996 (2013/07/25)

A simple and efficient method for the preparation of α,α- dichloroketones, α,α-dibromoketones, and α,α- diiodoketones by oxyhalogenation of alkynes using oxone and KX (X = Cl, Br, or I) is described.

Reactions of 2,2'-(Azo-2-phenoxypropane) with Bromine: a Novel Route to o- and p-Bromophenol

Kim, Kyongtae,Chang, Young-Chan

, p. 1159 - 1160 (2007/10/02)

o- and p-Bromophenol have been synthezied from the reactions of 2,2'-(azo-2-phenoxypropane) with different concentrations of bromine in 68 and 88percent yields, respectively.

3475-39-6 Process route

acetone
67-64-1

acetone

1,3-dibromoroacetone
816-39-7

1,3-dibromoroacetone

1,1,3-tribromoacetone
3475-39-6

1,1,3-tribromoacetone

1-bromoacetone
598-31-2

1-bromoacetone

Conditions
Conditions Yield
With pyridinium hydrobromide perbromide; In methanol; at 20 - 45 ℃; for 0.25h; Yield given. Yields of byproduct given;
 
1,1-dibromopropan-2-one
867-54-9

1,1-dibromopropan-2-one

water
7732-18-5

water

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

1,3-dibromoroacetone
816-39-7

1,3-dibromoroacetone

1,1,3-tribromoacetone
3475-39-6

1,1,3-tribromoacetone

1-bromoacetone
598-31-2

1-bromoacetone

Conditions
Conditions Yield
Gleichgewicht;
 

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  • 67-64-1
    67-64-1

    acetone

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