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522317

Sigma-Aldrich

2-Mercapto-4-methyl-5-thiazoleacetic acid

98%

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About This Item

Formula empirica (notazione di Hill):
C6H7NO2S2
Numero CAS:
34272-64-5
Peso molecolare:
189.26
Numero CE:
251-905-4
Numero MDL:
MFCD01750430
Codice UNSPSC:
12352100
ID PubChem:
24874264
NACRES:
NA.22

Livello qualitativo

100

Saggio

98%

Punto di fusione

207 °C (dec.) (lit.)

Gruppo funzionale

carboxylic acid

Stringa SMILE

Cc1nc(S)sc1CC(O)=O

InChI

1S/C6H7NO2S2/c1-3-4(2-5(8)9)11-6(10)7-3/h2H2,1H3,(H,7,10)(H,8,9)
KYBOCQHDFLVQIB-UHFFFAOYSA-N

Descrizione generale

2-Mercapto-4-methyl-5-thiazoleacetic acid is a thiazole derivative. It participates in the preparation of dinuclear [Au-(O4NCS2)]2 and tetranuclear [Au(SSCOOH)]4 complexes.

Applicazioni

2-Mercapto-4-methyl-5-thiazoleacetic acid may be used as a capping agent in the preparation of fused spherical gold nanoparticles. It may also be used in the synthesis of eight-tin macrocyclic complex (a 40-membered macrocycle containing two distannoxane ladders).

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKCM9123
MKCH8300
MKCG5459
MKCG1914
MKCB9278

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Chunlin Ma et al.
Dalton transactions (Cambridge, England : 2003), (12)(12), 1785-1786 (2004-09-24)
The self-assembly reaction of 2-mercapto-4-methyl-5-thiazoleacetic acid, sodium methoxide and dimethyltin dichloride in moist dichloromethane affords a novel eight-tin macrocyclic complex, which is a 40-membered macrocycle containing two distannoxane ladders.
P Kannan et al.
Analytica chimica acta, 663(2), 158-164 (2010-03-09)
We are reporting the highly sensitive determination of hydroxylamine (HA) using 2-mercapto-4-methyl-5-thiazoleacetic acid (TAA) capped fused spherical gold nanoparticles (AuNPs) modified Au electrode. The fused TAA-AuNPs were immobilized on (3-mercaptopropyl)-trimethoxysilane (MPTS) sol-gel film, which was pre-assembled on Au electrode. The
Chunlin Ma et al.
Inorganic chemistry, 47(16), 7060-7061 (2008-07-16)
The reaction of 1-(4-carboxyphenyl)-5-mercapto-1 H-tetrazole with trimethyltin chloride in the presence of sodium ethoxide in benzene affords a novel 2D organotin network structure complex 1, which is an unusual organotin network containing a hexanuclear 60-membered organotin macrocycle. The complex has
Dan Zhu et al.
Theranostics, 8(4), 941-954 (2018-02-22)
The recent proposition to combine liposomes with nanoparticles presents great opportunities to develop multifunctional drug delivery platforms. Although impressive progress has been made, attempts to elucidate the role nanoparticles play in the integral nanohybrids are still rather limited. Here, using
Isabel Freitag et al.
Journal of biomedical optics, 20(5), 55002-55002 (2015-05-06)
Identification of tumor and normal cells is a promising application of Raman spectroscopy. The throughput of Raman-assisted cell sorting is limited by low sensitivity. Surface-enhanced Raman spectroscopy (SERS) is a well-recognized candidate to increase the intensity of Raman signals of

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