Passa al contenuto
Merck
Tutte le immagini(1)

Documenti

163643

Sigma-Aldrich

N,N-Dimethylthioformamide

≥98%

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Formula condensata:
HCSN(CH3)2
Numero CAS:
Peso molecolare:
89.16
Beilstein:
1737191
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Livello qualitativo

Saggio

≥98%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.576 (lit.)

P. eboll.

58-60 °C/1 mmHg (lit.)

Densità

1.047 g/mL at 25 °C (lit.)

Stringa SMILE

[H]C(=S)N(C)C

InChI

1S/C3H7NS/c1-4(2)3-5/h3H,1-2H3
SKECXRFZFFAANN-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Descrizione generale

N,N-Dimethylthioformamide undergoes desulfurization reaction with hydrosilane under photo irradiation in the presence of a methyl iron complex. It forms a deep-orange complex with anhydrous bismuth(III) trifluoromethanesulfonate.

Applicazioni

N,N-Dimethylthioformamide was used as sulfur donor solvent to investigate the coordination chemistry of lead(II).

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

210.2 °F - closed cup

Punto d’infiammabilità (°C)

99 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

Krzysztof Lyczko et al.
Inorganic chemistry, 43(22), 7094-7100 (2004-10-27)
At the dissolution of anhydrous bismuth(III) trifluoromethanesulfonate in N,N-dimethylthioformamide (DMTF) a deep red-orange complex, lambda(max) = 457 nm, is formed. Bismuth(III) is reduced by the solvent to a low-valent oxidation state stabilized by the sulfur-coordinating solvent DMTF. The obtained complex
Ingmar Persson et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 22(51), 18583-18592 (2016-11-20)
The coordination chemistry of d10 s2 metal ions is strongly affected by an (at least partially) occupied d10 s2 metal ion-ligand atom antibonding orbital, which may cause a void in the coordination sphere due to repulsion between the electrons in
Kozo Fukumoto et al.
Chemical communications (Cambridge, England), 48(32), 3809-3811 (2012-01-06)
Desulfurization of N,N-dimethylthioformamide (Me(2)NCHS) by hydrosilane has been achieved under photo irradiation in the presence of a methyl iron complex. The reaction sequences have been proposed, in which silyl migration from Fe to S of thioformamide triggers the cleavage of
Ingmar Persson et al.
Inorganic chemistry, 50(3), 1058-1072 (2011-01-14)
The coordination chemistry of lead(II) in the oxygen donor solvents water, dimethylsulfoxide (dmso, Me(2)SO), N,N-dimethylformamide (dmf), N,N-dimethylacetamide (dma), N,N'-dimethylpropyleneurea (dmpu), and 1,1,3,3-tetramethylurea (tmu), as well as in the sulfur donor solvent N,N-dimethylthioformamide (dmtf), has been investigated by extended X-ray absorption

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.