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Merck
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Documenti fondamentali

T7641

Sigma-Aldrich

Tetrazole

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About This Item

Formula empirica (notazione di Hill):
CH2N4
Numero CAS:
Peso molecolare:
70.05
Beilstein:
105799
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:

Livello qualitativo

Punto di fusione

154-158 °C (lit.)

Stringa SMILE

c1nnn[nH]1

InChI

1S/CH2N4/c1-2-4-5-3-1/h1H,(H,2,3,4,5)
KJUGUADJHNHALS-UHFFFAOYSA-N

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Applicazioni

Not recommended for use in DNA synthesis.

Attenzione

Do not heat over 90°C (danger of explosion)

Pittogrammi

Exploding Bomb

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Self-react. A

Codice della classe di stoccaggio

1 - Explosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves


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Certificati d'analisi (COA)

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We investigated the effects of antitumor-active tetrazolato-bridged dinuclear platinum(II) complexes [{cis-Pt(NH(3))(2)}(2)(μ-OH)(μ-tetrazolato-N(1),N(2))](2+) (1) and [{cis-Pt(NH(3))(2)}(2)(μ-OH)(μ-tetrazolato-N(2),N(3))](2+) (2) on the higher-order structure of a large DNA molecule (T4 phage DNA, 166 kbp) in aqueous solution through single-molecule observation by fluorescence microscopy. Complexes 1
Duncan J Wardrop et al.
Organic letters, 14(6), 1548-1551 (2012-03-01)
The development of a mild, base-free method for the generation of alkylidenecarbenes is reported. Treatment of 5-hydroxyalkyl-1H-tetrazoles with carbodiimides generates products arising from the 1,2-rearrangement or [1,5]-C-H bond insertion of a putative alkylidenecarbene. Formation of this divalent intermediate is proposed
Mohamad Sabbah et al.
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New analogues of N-acyl-homoserine-lactone (AHL), in which the amide was replaced by a triazole or tetrazole ring, were prepared and tested for their activity as LuxR-dependent QS modulators. Several compounds showed a level of antagonistic or agonistic activity, notably some
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Journal of the American Chemical Society, 133(31), 11912-11915 (2011-07-09)
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ChemSusChem, 5(4), 647-651 (2012-03-06)
High-performance oxygen reduction reaction (ORR) catalysts based on metal-free nitrogen-containing precursors and carbon nanotubes are reported. The investigated systems allow the evaluation of the effect of nitrogen-containing groups towards ORR and the results show that the catalysts are compatible with

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