Metanilyl fluoride hydrochloride | CAS# 3887-48-7 | Biochemical

MedKoo Cat#: 577214 | Name: Metanilyl fluoride HCl

Description:

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

Metanilyl fluoride hydrochloride is a protease inhibitor.

Chemical Structure

Metanilyl fluoride HCl

CAS#3887-48-7

Theoretical Analysis

MedKoo Cat#: 577214

Name: Metanilyl fluoride HCl

CAS#: 3887-48-7

Chemical Formula: C6H7ClFNO2S

Exact Mass: 210.9870

Molecular Weight: 211.64

Elemental Analysis: C, 34.05; H, 3.33; Cl, 16.75; F, 8.98; N, 6.62; O, 15.12; S, 15.15

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Related CAS #

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Synonym

Metanilyl fluoride hydrochloride; Metanilyl fluoride HCl

IUPAC/Chemical Name

Benzenesulfonyl fluoride, 3-amino-, hydrochloride (1:1)

InChi Key

KTADZFWRDLKHKW-UHFFFAOYSA-N

InChi Code

InChI=1S/C6H6FNO2S.ClH/c7-11(9,10)6-3-1-2-5(8)4-6;/h1-4H,8H2;1H

SMILES Code

Cl.Nc1cccc(c1)S(=O)(=O)F

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

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

Instruction

View handling instruction

Preparing Stock Solutions

The following data is based on the product molecular weight 211.64 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.

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. Scozzafava A, Ilies MA, Manole G, Supuran CT. Protease inhibitors. Part 12. Synthesis of potent matrix metalloproteinase and bacterial collagenase inhibitors incorporating sulfonylated N-4-nitrobenzyl-beta-alanine hydroxamate moieties. Eur J Pharm Sci. 2000 Jul;11(1):69-79. doi: 10.1016/s0928-0987(00)00089-0. PMID: 10913755. 2. Scozzafava A, Supuran CT. Protease inhibitors: synthesis of potent bacterial collagenase and matrix metalloproteinase inhibitors incorporating N-4-nitrobenzylsulfonylglycine hydroxamate moieties. J Med Chem. 2000 May 4;43(9):1858-65. doi: 10.1021/jm990594k. PMID: 10794702.