357871
5-Mercapto-1-methyltetrazole
98%
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About This Item
Formule empirique (notation de Hill) :
C2H4N4S
Numéro CAS:
Poids moléculaire :
116.14
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
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Essai
98%
Forme
powder
Pf
125-128 °C (lit.)
Chaîne SMILES
Cn1nnnc1S
InChI
1S/C2H4N4S/c1-6-2(7)3-4-5-6/h1H3,(H,3,5,7)
Clé InChI
XOHZHMUQBFJTNH-UHFFFAOYSA-N
Description générale
5-Mercapto-1-methyltetrazole is a heterocyclic thiol derivative. It forms dimeric or tetrameric complexes with trimethylgallium.[1]
Application
5-Mercapto-1-methyltetrazole may be employed as heterocyclic ligand to study the geometry and stereochemical activity of the lone pair at the lead atom in hemi- and holo-directed lead(II) complexes.[2] It may be used in the chemical modification of submicron particles of mesoporous MSU-2 silica[3] and SBA-15 mesoporous silica.[4]
Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organes cibles
Respiratory system
Code de la classe de stockage
4.1A - Other explosive hazardous materials
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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Damián Pérez-Quintanilla et al.
Journal of nanoscience and nanotechnology, 9(8), 4901-4909 (2009-11-26)
Submicron particles of mesoporous MSU-2 silica have been obtained by using Tergitol NP-9 as nonionic surfactant and TEOS as silica precursor. The material has been chemically modified with 5-mercapto-1-methyltetrazole and characterized by powder X-ray diffraction, TEM, SEM, N2 adsorption, FT-IR
N Kanazumi et al.
Hepato-gastroenterology, 47(36), 1695-1699 (2001-01-10)
In this study, we examined the influence of clinical treatments in the perioperative period upon PIVKA-II (plasma levels of protein induced by vitamin K absence or antagonist-II) in patients with hepatocellular carcinoma and pancreatobiliary diseases. During a perioperative period, plasma
K Kawamoto et al.
Japanese journal of pharmacology, 47(2), 169-178 (1988-06-01)
Liver microsomal vitamin K epoxide reductase activity was determined by measuring the formation of menaquinone-4 from the substrate menaquinone-4 2,3-epoxide. The enzyme was active when dithiothreitol (DTT) was used as a reducing agent, and the activity increased gradually with increasing
Muhammad Imran et al.
Dalton transactions (Cambridge, England : 2003), 44(3), 924-937 (2014-08-12)
To investigate the geometry and stereochemical activity of the lone pair at the lead atom, lead(ii) complexes () with one tripodal (L(1)), one dipodal (L(2)) boron-centred soft ligand and eight other small soft heterocyclic ligands, 2-mercaptobenzimidazole (L(3)), 2-mercapto-5-methylbenzimidazole (L(4)), 3-mercapto-1,2,4-triazole
K Kawamoto et al.
Japanese journal of pharmacology, 50(2), 159-165 (1989-06-01)
NADH-dependent vitamin K reductase activity in rat liver microsomes was measured by detecting the amount of the reduced form of vitamin K from the oxidized form of the vitamin. The enzyme activity was not detected when intact microsomes were employed
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