What is the 5-Bromo-2-pyridinecarbonitrile?

5-Bromo-2-pyridinecarbonitrile is light yellow cryst, while it's Molecular Formula is C6H3BrN2. light yellow cryst 5-Bromo-2-pyridinecarbonitrile can be used in the synthesis of aza-terphenyl diamidine analogs, which exhibits potent antiprotozoal activity. It can also be used in the synthesis of pyridine-diketopyrrolopyrrole(PyDPP), a building block for preparing low band-gap copolymers for use as electron donor in polymer solar cells.

What is the CAS number for 5-Bromo-2-pyridinecarbonitrile?

The CAS number of 5-Bromo-2-pyridinecarbonitrile is 97483-77-7.

What is 5-Bromo-2-pyridinecarbonitrile (97483-77-7) used for?

5-Bromo-2-pyridinecarbonitrile is a light yellow crystalline compound that serves as an important intermediate in the synthesis of various organic compounds. It is characterized by the presence of a bromo and a nitrile group attached to a pyridine ring, which imparts unique chemical properties and reactivity to the molecule.InChI:InChI=1/C6H3BrN2/c7-5-1-2-6(3-8)9-4-5/h1-2,4H

What is the 5-Bromo-2-pyridinecarbonitrile?

5-Bromo-2-pyridinecarbonitrile is light yellow cryst, while it's Molecular Formula is C6H3BrN2. light yellow cryst 5-Bromo-2-pyridinecarbonitrile can be used in the synthesis of aza-terphenyl diamidine analogs, which exhibits potent antiprotozoal activity. It can also be used in the synthesis of pyridine-diketopyrrolopyrrole(PyDPP), a building block for preparing low band-gap copolymers for use as electron donor in polymer solar cells.

What is the CAS number for 5-Bromo-2-pyridinecarbonitrile?

The CAS number of 5-Bromo-2-pyridinecarbonitrile is 97483-77-7.

What is 5-Bromo-2-pyridinecarbonitrile (97483-77-7) used for?

5-Bromo-2-pyridinecarbonitrile is a light yellow crystalline compound that serves as an important intermediate in the synthesis of various organic compounds. It is characterized by the presence of a bromo and a nitrile group attached to a pyridine ring, which imparts unique chemical properties and reactivity to the molecule.InChI:InChI=1/C6H3BrN2/c7-5-1-2-6(3-8)9-4-5/h1-2,4H

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Product classification

97483-77-7

Product Name：2-cyano-5-bromopyridine
Molecular Formula：C₆H₃BrN₂
Purity：99%
Molecular Weight：183.007

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Product Details

pd_meltingpoint:128-132 °C(lit.)

Appearance:light yellow cryst

Purity:99%

Quality Manufacturer Supply High Purity 99% 2-cyano-5-bromopyridine 97483-77-7 with Reasonable Price

Molecular Formula:C6H3BrN2
Molecular Weight:183.007
Appearance/Colour:light yellow cryst
Vapor Pressure:0.0124mmHg at 25°C
Melting Point:128-132 °C(lit.)
Refractive Index:1.611
Boiling Point:260.3 °C at 760 mmHg
PKA:-2.68±0.10(Predicted)
Flash Point:111.2 °C
PSA：36.68000
Density:1.72 g/cm³
LogP:1.71578

5-Bromo-2-pyridinecarbonitrile(Cas 97483-77-7) Usage

InChI:InChI=1/C6H3BrN2/c7-5-1-2-6(3-8)9-4-5/h1-2,4H

97483-77-7 Relevant articles

Preparation method of 2-cyano-5-bromopyridine

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Paragraph 0035-0038; 0041-0045, (2021/11/06)

The invention provides a preparation met...

2 - Cyano -5 - bromo pyridine preparation method

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Paragraph 0025-0092, (2019/04/10)

The invention belongs to the field of or...

C?H Cyanation of 6-Ring N-Containing Heteroaromatics

Elbert, Bryony L.,Farley, Alistair J. M.,Gorman, Timothy W.,Johnson, Tarn C.,Genicot, Christophe,Lallemand, Bénédicte,Pasau, Patrick,Flasz, Jakub,Castro, José L.,MacCoss, Malcolm,Paton, Robert S.,Schofield, Christopher J.,Smith, Martin D.,Willis, Michael C.,Dixon, Darren J.

supporting information, p. 14733 - 14737 (2017/10/07)

Heteroaromatic nitriles are important co...

A oxazolidinone compounds of preparation method (by machine translation)

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Paragraph 0048, (2017/05/12)

The invention provides a oxazolidinone c...

97483-77-7 Process route

: 624-28-2
2,5-dibromopyridine

: 97483-77-7
2-Cyano-5-bromopyridine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1.1: 85 percent / NaI; AcCl / acetonitrile / 3 h / Heating 2.1: iPrMgCl / CH₂Cl₂; tetrahydrofuran / 0.75 h / 0 °C 2.2: 82 percent / CH₂Cl₂; tetrahydrofuran / 2 h / 20 °C With isopropylmagnesium chloride; acetyl chloride; sodium iodide; In tetrahydrofuran; dichloromethane; acetonitrile;
Multi-step reaction with 2 steps 1.1: n-butyllithium / toluene / 2 h / -78 °C 1.2: toluene / 1 h / -78 °C 2.1: POCl₃ / toluene / 5 h / 110 °C With n-butyllithium; trichlorophosphate; In toluene;
In N-methyl-acetamide;
With zinc(II) cyanide; zinc; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In DMF (N,N-dimethyl-formamide); for 5h; Heating / reflux;