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Sigma-Aldrich

Benzamide

purified by sublimation, ≥99.5%

Sinônimo(s):

Benzoic acid amide

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About This Item

Fórmula linear:
C6H5CONH2
Número CAS:
55-21-0
Peso molecular:
121.14
Beilstein:
385876
Número CE:
200-227-7
Número MDL:
MFCD00007968
Código UNSPSC:
12352100
ID de substância PubChem:
24864807
NACRES:
NA.22

Ensaio

≥99.5%

forma

powder

purificado por

sublimation

pf

125-128 °C (lit.)

solubilidade

ethanol: soluble 50 mg/mL, clear to slightly hazy, colorless to light yellow

cadeia de caracteres SMILES

NC(=O)c1ccccc1

InChI

1S/C7H7NO/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)

chave InChI

KXDAEFPNCMNJSK-UHFFFAOYSA-N

Informações sobre genes

human ... PARP1(142)

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Categorias relacionadas

Descrição geral

Benzamide (Benzoic acid amide, BA) is an amide of benzoic acid. BA on crystallization in benzene (solvent) affords crystals suitable for X-ray analysis. Crystal structure studies suggest that its crystals are monoclinic having space group P21/c. Kinetics and mechanism of its reaction with hydrogen peroxide have been proposed.

Aplicação

Benzamide was used to study the mechanism of photocatalytic decomposition of aqueous solution of acetic acid, acetamide and acetonitrile in the presence of semiconductors. Benzamide was used to develop a robust screening method to study biotransformations using (+)-γ-lactamase enzyme.

Ações bioquímicas/fisiológicas

Inhibits poly(ADP-ribose) polymerase (PARP).

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Warning

Frases de perigo

H302,H341

Classificações de perigo

Acute Tox. 4 Oral - Muta. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

356.0 °F - closed cup

Ponto de fulgor (°C)

180 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

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The mechanisms of hydrogen peroxide reactions. I. The conversion of benzonitrile to benzamide.
Wiberg KB.
Journal of the American Chemical Society, 75(16), 3961-3964 (1953)
The crystal and molecular structure of benzamide.
Penfold BR and White JCB.
Acta Crystallographica, 12(2), 130-135 (1959)
Photocatalytic Decompositions of Carboxylic Acid Derivatives by Semiconductors.
Park KH and Kim JH.
Bull. Korean Chem. Soc., 12(4), 439-439 (1991)
Anne Marie Hickey et al.
Biotechnology journal, 4(4), 510-516 (2009-03-18)
A (+)-gamma-lactamase was precipitated, cross-linked and the resulting solid crushed prior to immobilisation within a capillary column microreactor. The microreactor was subsequently used to study enzyme stability, activity, kinetics and substrate specificity. The thermophilic (+)-gamma-lactamase retained 100% of its initial
Walter Mier et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 55(1), 9-14 (2013-11-28)
The performance of cytotoxic drugs is defined by their selectivity of uptake and action in tumor tissue. Recent clinical responses achieved by treating metastatic malignant melanoma with therapeutic modalities based on gene expression profiling showed that malignant melanoma is amenable
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