CAS 614-76-6

N-(2-Bromophenyl)acetamide

Description:

N-(2-Bromophenyl)acetamide, with the CAS number 614-76-6, is an organic compound characterized by the presence of a bromine atom attached to a phenyl ring, which is further substituted by an acetamide group. This compound typically appears as a solid and is known for its moderate solubility in organic solvents. The presence of the bromine atom contributes to its reactivity, making it useful in various chemical synthesis processes, particularly in the development of pharmaceuticals and agrochemicals. The acetamide functional group imparts certain polar characteristics, influencing its interactions and solubility in different media. N-(2-Bromophenyl)acetamide can participate in nucleophilic substitution reactions and may serve as a precursor for more complex organic molecules. Safety considerations should be taken into account when handling this compound, as it may pose health risks if ingested or inhaled, and appropriate safety measures should be implemented in laboratory settings. Overall, its unique structural features make it a valuable compound in organic chemistry research and applications.

Formula: C₈H₈BrNO

InChI: InChI=1S/C8H8BrNO/c1-6(11)10-8-5-3-2-4-7(8)9/h2-5H,1H3,(H,10,11)

InChI key: InChIKey=VOBKUOHHOWQHFZ-UHFFFAOYSA-N

SMILES: N(C(C)=O)C1=C(Br)C=CC=C1

Synonyms:

• 2-(Acetylamino)bromobenzene
• 2-Bromo-N-acetylaniline
• Acetamide, N-(2-bromophenyl)-
• Acetanilide, 2′-bromo-
• N-(2-bromophenyl)acetamide
• N-Acetyl-2-bromoaniline
• o-Bromoacetanilide
• 2′-Bromoacetanilide

2'-Bromoacetanilide

CAS: 614-76-6

Formula: C₈H₈BrNO

Purity: >98.0%(GC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 214.06

Ref: 3B-B3139

N-(2-Bromophenyl)acetamide

CAS: 614-76-6

Formula: C₈H₈BrNO

Purity: 98%

Color and Shape: Solid

Molecular weight: 214.0592

Ref: IN-DA003B6M

2'-Bromoacetanilide

CAS: 614-76-6

2'-Bromoacetanilide

Formula: C₈H₈BrNO

Purity: ≥95%

Color and Shape: white crystalline needles

Molecular weight: 214.06g/mol

Ref: 54-OR4339

2'-Bromoacetanilide

Controlled Product

CAS: 614-76-6

Applications 2'-Bromoacetanilide is used as a reagent in the preparation of furan-2-ylmethylene thiazolidinediones as novel, potent, and selective inhibitors of phosphoinositide 3-kinase γ.
References Pomel, V., et al.: J. Med. Chem., 49, 3857 (2006);

Formula: C₈H₈BrNO

Color and Shape: Neat

Molecular weight: 214.06

Ref: TR-B679010

N-(2-Bromophenyl)acetamide

CAS: 614-76-6

Formula: C₈H₈BrNO

Purity: 98%

Color and Shape: Solid

Molecular weight: 214.062

Ref: 10-F224327

2'-Bromoacetanilide

CAS: 614-76-6

2'-Bromoacetanilide is a carbazole compound that can be synthesized in two steps from 2-bromoacetamide. The first step involves the reaction of 2-bromoacetamide with carbon tetrachloride and phosphine, followed by the addition of an amine to produce a palladium complex. This complex reacts with carbon nanotubes to form the desired product, 2'-bromoacetanilide. The catellani reaction is a chemical reaction that involves the formation of an amide bond between an amine and an aldehyde or ketone. The diazonium salt is generated from the coupling of hydrogen peroxide and nitrite ions, which then react with phenol to form the desired product.
2'-Bromoacetanilide has been shown to undergo cross-coupling reactions with various functional groups such as acids, alcohols, and halides to form different products. Struct

Formula: C₈H₈BrNO

Purity: Min. 95%

Molecular weight: 214.06 g/mol

Ref: 3D-AAA61476