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5-Mercapto-1-methyltetrazol
98%
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About This Item
Empirische Formel (Hill-System):
C2H4N4S
CAS-Nummer:
Molekulargewicht:
116.14
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Assay
98%
Form
powder
mp (Schmelzpunkt)
125-128 °C (lit.)
SMILES String
Cn1nnnc1S
InChI
1S/C2H4N4S/c1-6-2(7)3-4-5-6/h1H3,(H,3,5,7)
InChIKey
XOHZHMUQBFJTNH-UHFFFAOYSA-N
Allgemeine Beschreibung
5-Mercapto-1-methyltetrazole is a heterocyclic thiol derivative. It forms dimeric or tetrameric complexes with trimethylgallium.[1]
Anwendung
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]
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
4.1A - Other explosive hazardous materials
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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Adriana Ilie et al.
Inorganic chemistry, 50(6), 2675-2684 (2011-02-12)
Gold(I) and silver(I) complexes of 1-methyl-5-thio-tetrazole (1) have been prepared and the coordination chemistry of this ligand toward metal-phosphine frameworks has been explored. As indicated by IR and Raman data, ligand 1 is deprotonated and the resulted anion acts as
T F Goss et al.
Pharmacotherapy, 12(4), 283-291 (1992-01-11)
A prospective surveillance program was initiated to determine the relative role of antibiotics containing N-methylthiotetrazole (NMTT) versus patient risk factors in producing antibiotic-associated bleeding. Five hundred forty-six critically ill patients with serum albumin 30 g/L or below were evaluated for
Damián Pérez-Quintanilla et al.
Journal of separation science, 30(10), 1556-1567 (2007-07-12)
In this work, a mesoporous silica has been chemically modified with 5-mercapto-1-methyl-1-H-tetrazol using the homogeneous route (MTTZ-HMS). This synthetic route involved the reaction of 5-mercapto-1-methyl-1-H-tetrazol with 3-chloropropyltriethoxysilane, prior to immobilization on the support. The resulting material has been characterized and
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
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