MedKoo Cat#: 534803 | Name: Naproanilide

Description:

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

Naproanilide is an agricultural herbicide chemical.

Chemical Structure

Naproanilide
Naproanilide
CAS#52570-16-8

Theoretical Analysis

MedKoo Cat#: 534803

Name: Naproanilide

CAS#: 52570-16-8

Chemical Formula: C19H17NO2

Exact Mass: 291.1259

Molecular Weight: 291.35

Elemental Analysis: C, 78.33; H, 5.88; N, 4.81; O, 10.98

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
Naproanilide
IUPAC/Chemical Name
Propanamide, 2-(2-naphthalenyloxy)-N-phenyl-
InChi Key
LVKTWOXHRYGDMM-UHFFFAOYSA-N
InChi Code
InChI=1S/C19H17NO2/c1-14(19(21)20-17-9-3-2-4-10-17)22-18-12-11-15-7-5-6-8-16(15)13-18/h2-14H,1H3,(H,20,21)
SMILES Code
CC(OC1=CC=C2C=CC=CC2=C1)C(NC3=CC=CC=C3)=O
Appearance
Solid powder
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
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
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 291.35 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
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Two new aminopeptidases from Ochrobactrum anthropi active on D-alanyl-p-nitroanilide. Cell Mol Life Sci. 1999 May;55(5):812-8. doi: 10.1007/s000180050334. PMID: 10379365. 12: Tanaka T, McRae BJ, Cho K, Cook R, Fraki JE, Johnson DA, Powers JC. Mammalian tissue trypsin-like enzymes. Comparative reactivities of human skin tryptase, human lung tryptase, and bovine trypsin with peptide 4-nitroanilide and thioester substrates. J Biol Chem. 1983 Nov 25;258(22):13552-7. PMID: 6358206. 13: Pelletier A, Dimicoli JL, Boudier C, Bieth JG. Nonchromogenic hydrolysis of elastase and cathepsin G p-nitroanilide substrates by Pseudomonas aeruginosa elastase. Am J Respir Cell Mol Biol. 1989 Jul;1(1):37-9. doi: 10.1165/ajrcmb/1.1.37. PMID: 2516450. 14: Shechter Y, Gertler A. Enhancement of alpha-chymotrypsin-catalyzed hydrolysis of specific p-nitroanilide substrates by 4-phenylbutylamine derivative of hen egg-white lysozyme. 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PMID: 2317934. 18: Magalhães HP, Magalhães A, Juliano L, Nelson DL, Rogana E. Mechanism of action and determination of the best substrate for a thrombin-like enzyme from Lachesis muta muta venom by regression analysis of the kinetic parameters determined with peptidyl p-nitroanilide substrates. Toxicon. 2006 Mar 15;47(4):453-8. doi: 10.1016/j.toxicon.2006.01.001. Epub 2006 Feb 20. PMID: 16488459. 19: Sousa MO, Miranda TL, Maia CN, Bittar ER, Santoro MM, Figueiredo AF. Kinetic peculiarities of human tissue kallikrein: 1--substrate activation in the catalyzed hydrolysis of H-D-valyl-L-leucyl-L-arginine 4-nitroanilide and H-D- valyl-L-leucyl-L-lysine 4-nitroanilide; 2--substrate inhibition in the catalyzed hydrolysis of N alpha-p-tosyl-L-arginine methyl ester. Arch Biochem Biophys. 2002 Apr 1;400(1):7-14. doi: 10.1006/abbi.2002.2764. PMID: 11913965. 20: Ohlsson BG, Weström BR, Karlsson BW. 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