13881-91-9 Usage
Description
Aminomethanesulfonic acid, also known as mesitylenesulfonamide or methanesulfonamide, is an organic compound with the chemical formula CH3NHSO3H. It is a white powder that serves as a versatile reactant in various chemical syntheses and functionalization processes.
Uses
Used in Pharmaceutical Industry:
Aminomethanesulfonic acid is used as a reactant for the synthesis of 1-Sulfomethyltetrazole-5-thiol disodium salts, which are key intermediates in the preparation of cefonicid sodium, an antibiotic.
Used in Chemical Synthesis:
Aminomethanesulfonic acid is used as a reactant to synthesize tridentate N-(2-hydroxybenzyl)aminomethane sulfonic acid Schiff-base ligand by reacting with salicylaldehyde, which can be utilized in various chemical applications.
Used in Material Science:
Aminomethanesulfonic acid is used to functionalize the surface of single-walled carbon nanotubes (SWCNT) or porous metal-organic frameworks (MOF) by introducing sulfonic acid functional groups. This functionalization process is essential for the preparation of nanocomposites with enhanced properties and potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 13881-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,8 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13881-91:
(7*1)+(6*3)+(5*8)+(4*8)+(3*1)+(2*9)+(1*1)=119
119 % 10 = 9
So 13881-91-9 is a valid CAS Registry Number.
InChI:InChI=1/CH5NO3S/c2-1-6(3,4)5/h1-2H2,(H,3,4,5)
13881-91-9Relevant articles and documents
Features of interaction in the sulfur(IV) oxide-hexamethylenetetramine- water system: A first example of identification of the product with a sulfur-carbon bond
Khoma,Shestaka,Shishkin,Baumer,Brusilovskii, Yu. E.,Koroeva,Ennan,Gel'mbol'D
, p. 620 - 621 (2011)
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1,5-EPOXY-2,3,4,5-TETRAHYDRO-1H-3-BENZAZEPINS AND USE IN TREATMENT OF ULCERS
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, (2008/06/13)
The synthesis of epoxybenzazepin compounds is described. The novel compounds have anti-ulcer activity.
Probiotics. Antistaphylococcal and antifibrinolytic activities of omega amino and omega guanidinoalkanesulfonic acids
Fujii,Cook
, p. 502 - 505 (2007/10/05)
A series of ;. aminoalkanesulfonic acid and ω guanidinoalkanesulfonic acids was tested for antistaphylococcal and antifibrinolytic activities. Most of the former and one of the latter class gave better protection against Staphylococcus aureus infections in mice than 4 aminobutyryl L histidine. Most of the ω aminoalkanesulfonic acids showed antifibrinolytic activity, one of them having activity equal to or greater than that of aminocaproic acid, whereas none of the ω guanidinoalkanesulfonic acids had significant antifibrinolytic activity.