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ChemicalBook--->CAS DataBase List--->156001-51-3

156001-51-3

156001-51-3 Structure

156001-51-3 Structure
IdentificationBack Directory
[Name]

5-BROMO-2-METHYLBENZONITRILE
[CAS]

156001-51-3
[Synonyms]

4-Bromo-2-cyanotoluene
Bromo-2-methylbenzonitrile
3-BROMO-6-METHYLBENZONITRILE
5-BROMO-2-METHYLBENZONITRILE
5-Bromo-2-methylbenzonotrile
2-Methyl-5-bBromobenzonitrile
Benzonitrile, 5-bromo-2-methyl-
5-BROMO-2-METHYLBENZONITRILE,98%
[Molecular Formula]

C8H6BrN
[MDL Number]

MFCD08061920
[MOL File]

156001-51-3.mol
[Molecular Weight]

196.04
Chemical PropertiesBack Directory
[Melting point ]

47-51 °C
[Boiling point ]

251℃
[density ]

1.51
[Fp ]

110 °C
[storage temp. ]

Room temperature.
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[color ]

White to Orange to Green
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[RIDADR ]

UN 3439 6.1/PG III
[WGK Germany ]

3
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

2926907090
Hazard InformationBack Directory
[Uses]

2-Hydroxy-6-methyl-5-nitropyridine is a versatile building block that can be used to create a range of compounds, such as 5-Bromo-2-methylbenzaldehyde, 1-(5-Bromo-2-methylphenyl)ethanone, etc.
[Reactions]

5-Bromo-2-methylbenzonitrile is a substrate for the enzyme benzoate kinase and is used as an intermediate in the synthesis of cyclen. It can be activated by addition of acid, which leads to a rapid increase in the rate of reaction. The kinetic data for this reaction have been analyzed and show that it obeys first order kinetics with respect to both 5-bromo-2-methylbenzonitrile and benzoic acid. This reaction is also catalyzed by an analog of cyclen, which binds to the enzyme more tightly than 5-bromo-2-methylbenzonitrile, resulting in a higher activation energy. It is possible to analyze the kinetics of this reaction using agarose gel electrophoresis or supercoiled DNA analysis.
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