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135828

Sigma-Aldrich

Benzamid

99%

Synonym(e):

Benzoesäureamid

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About This Item

Lineare Formel:
C6H5CONH2
CAS-Nummer:
55-21-0
Molekulargewicht:
121.14
Beilstein:
385876
EG-Nummer:
200-227-7
MDL-Nummer:
MFCD00007968
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24848219
NACRES:
NA.22

Qualitätsniveau

100

Assay

99%

mp (Schmelzpunkt)

125-128 °C (lit.)

Löslichkeit

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

SMILES String

NC(=O)c1ccccc1

InChI

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

InChIKey

KXDAEFPNCMNJSK-UHFFFAOYSA-N

Angaben zum Gen

human ... PARP1(142)

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Allgemeine Beschreibung

Benzamide on radioiodination by different labeling procedures results in large-scale production of radioiodinated benzamides having potential therapeutic application for patients with metastatic malignant melanoma.

Benzamide is used as a building block in organic synthesis for the preparation of various biologically active compounds.

Anwendung

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

Biochem./physiol. Wirkung

Inhibiert Poly(ADP-Ribose)-Polymerase (PARP)

Piktogramme

Health hazardExclamation mark
GHS08,GHS07

Signalwort

Warning

H-Sätze

H302,H341

Gefahreneinstufungen

Acute Tox. 4 Oral - Muta. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

356.0 °F - closed cup

Flammpunkt (°C)

180 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

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Dichlormethan anhydrous, ≥99.8%, contains 40-150 ppm amylene as stabilizer

Sigma-Aldrich

270997

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(1R,3S)-(+)-Kampfersäure 99%

Sigma-Aldrich

C409

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Sigma-Aldrich

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m-Tolunsäure

Chapter One-Recent Advances in Cancer Therapeutics
Nicola, et al.
Progress in Medicinal Chemistry, 54 null
Willian G Birolli et al.
Pesticide biochemistry and physiology, 156, 129-137 (2019-04-28)
Chiral pesticides have been used in agriculture, including (±)-lambda-cyhalothrin ((±)-LC), which is a pyrethroid insecticide widely employed on crops for protection against different types of insects. However, enantioselectivity is poorly studied in biodegradation processes. Therefore, the (±)-LC enantioselective biodegradation by
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
Photocatalytic Decompositions of Carboxylic Acid Derivatives by Semiconductors.
Park KH and Kim JH.
Bull. Korean Chem. Soc., 12(4), 439-439 (1991)
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