• Product Name2-BROMO-5-HYDROXYBENZALDEHYDE
  • CasNo. 2973-80-0
  • MFC7H5BrO2
  • MW201.019
  • Purity
  • Appearance
  • Packing
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Product Details

CasNo: 2973-80-0

MF: C7H5BrO2

Manufacturer supply high quality 2-BROMO-5-HYDROXYBENZALDEHYDE 2973-80-0 with GMP standards

  • Molecular Formula:C7H5BrO2
  • Molecular Weight:201.019
  • Vapor Pressure:0.00151mmHg at 25°C 
  • Melting Point:130-135 °C 
  • Refractive Index:1.657 
  • Boiling Point:286.7 °C at 760 mmHg 
  • PKA:8.67±0.18(Predicted) 
  • Flash Point:127.2 °C 
  • PSA:37.30000 
  • Density:1.737 g/cm3 
  • LogP:1.96720 

2-BROMO-5-HYDROXYBENZALDEHYDE(Cas 2973-80-0) Usage

InChI:InChI=1/C7H5BrO2/c8-7-2-1-6(10)3-5(7)4-9/h1-4,10H

2973-80-0 Relevant articles

Synthesis of Complex Stereoheptads en Route to Daphnane Diterpene Orthoesters

Nguyen, Long V.,Beeler, Aaron B.

, p. 5177 - 5180 (2018)

Tricyclic cores of the daphnane diterpen...

2-Bromo-5-hydroxybenzaldehyde

Matos Beja,Paixao,Ramos Silva,Alte Da Veiga,Rocha Gonsalves,Serra

, p. 354 - 355 (2000)

The molecules of the title compound, C7H...

Synthesis of new Zn (II) complexes for photo decomposition of organic dye pollutants, industrial wastewater and photo-oxidation of methyl arenes under visible-light

Ahemed, Jakeer,Bhongiri, Yadagiri,Chetti, Prabhakar,Gade, Ramesh,Kore, Ranjith,Pasha, Jakeer,Pola, Someshwar,Rao D, Venkateshwar

, (2021/07/28)

Synthesis of new Schiff's base Zn-comple...

Optimization of Manganese Coupling Reaction for Kilogram-Scale Preparation of Two Aryl-1,3-dione Building Blocks

Smejkal, Tomas,Gopalsamuthiram, Vijayagopal,Ghorai, Sujit K.,Jawalekar, Anup M.,Pagar, Dinesh,Sawant, Krishna,Subramanian, Srinivas,Dallimore, Jonathan,Willetts, Nigel,Scutt, James N.,Whalley, Louisa,Hotson, Matthew,Hogan, Anne-Marie,Hodges, George

, p. 1625 - 1632 (2017/10/25)

Aryl-1,3-diones represent a promising ne...

Identification of the Iodination and Bromination Products of 3-Hydroxybenzaldehyde: Preparation of 5-Hydroxy-2-iodobenzaldehyde

Blasco, Raül,de Arellano, Carmen Ramírez,Sanz-Cervera, Juan F.

, p. 265 - 272 (2017/06/09)

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2973-80-0 Process route

meta-hydroxybenzaldehyde
100-83-4

meta-hydroxybenzaldehyde

2-bromo-5-hydroxybenzaldehyde
2973-80-0

2-bromo-5-hydroxybenzaldehyde

5-formyl-2-nitrophenol
704-13-2

5-formyl-2-nitrophenol

Conditions
Conditions Yield
With nitric acid; potassium bromide; In acetic anhydride; at 20 ℃;
39 %Chromat.
35 %Chromat.
meta-hydroxybenzaldehyde
100-83-4

meta-hydroxybenzaldehyde

2-bromo-5-hydroxybenzaldehyde
2973-80-0

2-bromo-5-hydroxybenzaldehyde

Conditions
Conditions Yield
With bromine; In dichloromethane;
100%
With bromine; In dichloromethane;
100%
With 1,3-di-n-butyl-1H-imidazol-3-ium tribromide; at 20 ℃; for 0.133333h; regioselective reaction; Neat (no solvent);
95%
With 1-butyl-3-methylpyridinium tribromide; at 20 ℃; for 0.25h;
92%
With 1,4-dioxane dibromide; at 20 ℃; for 0.5h;
80%
With bromine; iron; In acetic acid; at 20 ℃;
80%
With bromine; In chloroform; acetonitrile; for 3.5h;
78%
With bromine; In tetrachloromethane; for 2.25h;
76%
With bromine; In dichloromethane; at 0 - 2 ℃; for 17h;
76%
With bromine; In dichloromethane; at 0 - 20 ℃; for 5h;
75%
With bromine; In dichloromethane; at -5 - 25 ℃; for 15h; Inert atmosphere; Large scale;
74%
With bromine; In chloroform; for 3h; Ambient temperature;
73%
With bromine; In acetic acid; for 3h;
68%
With bromine; In dichloromethane; Reflux; Large scale;
65%
With bromine; In dichloromethane;
63%
With bromine; In dichloromethane; at 35 - 40 ℃;
63%
With bromine; acetic acid;
57%
With bromine; In dichloromethane; at 20 ℃; for 1.5h; Inert atmosphere;
56%
With bromine; acetic acid; at 15 - 22 ℃;
55%
With bromine; acetic acid; at 20 ℃;
55%
With bromine; In chloroform; acetonitrile; at 20 ℃; for 4h; Cooling with ice;
55%
With bromine; In tetrachloromethane; at 20 ℃; for 2h;
51%
With bromine; sodium carbonate; In chloroform;
50%
With bromine; In dichloromethane; at 25 ℃; for 12h; Inert atmosphere;
49%
With bromine; In dichloromethane; for 3h; Ambient temperature;
45%
With bromine; acetic acid; at 10 - 20 ℃; for 2.66667h; Inert atmosphere;
35%
durch Bromierung;
With chloroform; bromine;
With bromine; acetic acid;
With bromine; In chloroform; at 25 ℃;
Multi-step reaction with 2 steps
1: bei der Nitrierung
2: Na2S2O4; water / Diazotieren in bromwasserstoffsaurer Loesung und nachfolgende Behandlung mit Kupfer(I)-bromid
With sodium dithionite; water;
With bromine;

2973-80-0 Upstream products

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    2-nitro-5-hydroxybenzaldehyde

  • 100-83-4
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    meta-hydroxybenzaldehyde

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    3-Benzyloxybenzaldehyde

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2973-80-0 Downstream products

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    2-bromo-5-methoxy-benzaldehyde

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    2-bromo-5-(3-thiophen-3-yl-methyloxy)benzaldehyde

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