CAS 3013-38-5

2,4-Dinitrobenzylbromide

Description:

2,4-Dinitrobenzylbromide, with the CAS number 3013-38-5, is an organic compound characterized by its aromatic structure and the presence of both nitro and bromine functional groups. It features a benzene ring substituted at the 2 and 4 positions with nitro groups, which are electron-withdrawing, and at the 1 position with a bromine atom. This compound is typically a yellow crystalline solid, indicating its potential for applications in organic synthesis and as a reagent in various chemical reactions. The presence of the nitro groups enhances its electrophilic character, making it reactive towards nucleophiles. Additionally, 2,4-Dinitrobenzylbromide is known for its use in the synthesis of other chemical compounds, particularly in the preparation of dinitrophenyl derivatives. It is important to handle this compound with care due to its potential toxicity and environmental impact, as well as the hazards associated with its nitro groups, which can be explosive under certain conditions. Proper safety protocols should be followed when working with this substance in a laboratory setting.

Formula: C₇H₅BrN₂O₄

InChI: InChI=1/C7H5BrN2O4/c8-4-5-1-2-6(9(11)12)3-7(5)10(13)14/h1-3H,4H2

SMILES: c1cc(cc(c1CBr)N(=O)=O)N(=O)=O

Synonyms:

• 1-(Bromomethyl)-2,4-Dinitrobenzene

2,4-DINITROBENZYL BROMIDE

CAS: 3013-38-5

Formula: C₇H₅BrN₂O₄

Purity: 98%

Color and Shape: Liquid

Molecular weight: 261.0296

Ref: IN-DA00383B

1-(Bromomethyl)-2,4-Dinitrobenzene

CAS: 3013-38-5

1-(Bromomethyl)-2,4-Dinitrobenzene

Purity: 98%

Molecular weight: 261.03g/mol

Ref: 54-OR1024601

2,4-Dinitrobenzyl Bromide

Controlled Product

CAS: 3013-38-5

Applications 2,4-DINITROBENZYL BROMIDE (cas# 3013-38-5) is a useful research chemical.

Formula: C₇H₅BrN₂O₄

Color and Shape: Yellow

Molecular weight: 261.03

Ref: TR-D680470

1-(Bromomethyl)-2,4-dinitrobenzene

CAS: 3013-38-5

1-(Bromomethyl)-2,4-dinitrobenzene is a phenacyl derivative that can be used for the synthesis of β-unsaturated aldehydes. It is activated with chloride and reacted with various halides to generate the desired product. 1-(Bromomethyl)-2,4-dinitrobenzene has been shown to react with photoexcited acceptors such as benzophenone and tetrachloroethene to produce trisubstituted products. The mechanistic study of this compound provides insight into the activation process and the resulting products.

Formula: C₇H₅BrN₂O₄

Purity: Min. 95%

Molecular weight: 261.03 g/mol

Ref: 3D-DAA01338