MedKoo Cat#: 145860 | Name: Oxanilide

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Oxanilide is an organic compound used primarily in the field of chemistry as an intermediate in the synthesis of various chemical products, including pharmaceuticals and dyes. It has been explored for its potential in antimicrobial and antifungal applications, where it can help inhibit the growth of certain pathogens. The mechanism of oxanilide involves its ability to interfere with the cellular processes of microorganisms, preventing their proliferation and reducing infection. In industrial applications, it serves as a key component in producing other compounds and enhancing product stability.

Chemical Structure

Oxanilide
Oxanilide
CAS#620-81-5

Theoretical Analysis

MedKoo Cat#: 145860

Name: Oxanilide

CAS#: 620-81-5

Chemical Formula: C14H12N2O2

Exact Mass: 240.0900

Molecular Weight: 240.26

Elemental Analysis: C, 69.99; H, 5.03; N, 11.66; O, 13.32

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Oxanilide; NSC-4183; NSC4183; NSC 4183; AI3-00844; AI3 00844; AI300844;
IUPAC/Chemical Name
N1,N2-diphenyloxalamide
InChi Key
FTWUXYZHDFCGSV-UHFFFAOYSA-N
InChi Code
1S/C14H12N2O2/c17-13(15-11-7-3-1-4-8-11)14(18)16-12-9-5-2-6-10-12/h1-10H,(H,15,17)(H,16,18)
SMILES Code
O=C(NC1=CC=CC=C1)C(=O)NC2=CC=CC=C2
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 240.26 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: PRICE CC, VELZEN BH. Some derivatives of oxanilide. J Org Chem. 1947 May;12(3):386-92. doi: 10.1021/jo01167a005. PMID: 20240580. 2: Tayabali AF, Seligy VL. Semiautomated quantification of cytotoxic damage induced in cultured insect cells exposed to commercial Bacillus thuringiensis biopesticides. J Appl Toxicol. 1995 Sep-Oct;15(5):365-73. doi: 10.1002/jat.2550150505. PMID: 8666719. 3: Leeson PD, Baker R, Carling RW, Curtis NR, Moore KW, Williams BJ, Foster AC, Donald AE, Kemp JA, Marshall GR. Kynurenic acid derivatives. Structure-activity relationships for excitatory amino acid antagonism and identification of potent and selective antagonists at the glycine site on the N-methyl-D-aspartate receptor. J Med Chem. 1991 Apr;34(4):1243-52. doi: 10.1021/jm00108a002. PMID: 1826744. 4: Kairo SK, Bedwell J, Tyler PC, Carter A, Corbel MJ. Development of a tetrazolium salt assay for rapid determination of viability of BCG vaccines. Vaccine. 1999 May 14;17(19):2423-8. doi: 10.1016/s0264-410x(99)00023-7. PMID: 10392624. 5: Nosaka C, Kunimoto S, Takeuchi T. The decrease of cytochrome c oxidase activity by 15-deoxyspergualin results in enhancement of XTT reduction in cultured cells. J Antibiot (Tokyo). 1999 Sep;52(9):803-8. doi: 10.7164/antibiotics.52.803. PMID: 10726928.