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Merck

125571

Sigma-Aldrich

5-Chloro-2-mercaptobenzothiazole

technical grade, ≥90%

Sinónimos:

CMBT

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About This Item

Fórmula empírica (notación de Hill):
C7H4ClNS2
Número de CAS:
Peso molecular:
201.70
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22

grado

technical grade

Nivel de calidad

Ensayo

≥90%

mp

198-200 °C (lit.)

grupo funcional

chloro

cadena SMILES

Sc1nc2cc(Cl)ccc2s1

InChI

1S/C7H4ClNS2/c8-4-1-2-6-5(3-4)9-7(10)11-6/h1-3H,(H,9,10)

Clave InChI

NKYDKCVZNMNZCM-UHFFFAOYSA-N

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Descripción general

5-Chloro-2-mercaptobenzothiazole(CMBZT) reacts with iodine in a molar ratio of 1:1 to form charge-transfer complex (CMBZT)I2.

Aplicación

5-Chloro-2-mercaptobenzothiazole (CMBZT) has been used in the analysis of lipopolysaccharide by negative-ion matrix-assisted laser desorption ionization-time of flight mass spectrometry. It has been used in the synthesis of the new mixed ligand silver(I) chloride complex with the heterocyclic thioamide CMBZT and tri(p-tolyl)phosphine. Found to be more sensitive than DHB for analysis of high mannose N-linked glycans. Used in analysis of peptidoglycan muropeptides.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Synthesis and Characterization of (PTU) I2 (PTU= 6-n-propyl-2-thiouracil) and (CMBZT) I2 (CMBZT= 5-chloro-2-mercaptobenzothiazole) and Possible Implications for the Mechanism of Action of Anti-Thyroid Drugs.
Antoniadis CD, et al.
European Journal of Inorganic Chemistry, 2003(8), 1635-1640 (2003)
L Kyros et al.
Bioinorganic chemistry and applications, 386860-386860 (2010-04-10)
The synthesis and characterization of the silver(I) chloride complex of formula {[AgCI(CMBZT)(TPTP)(2)] . (MeOH)} (1) (CMBZT = 5-chloro-2-mercaptobenzothiazole, TPTP = tris(p-tolyl)phosphine) is described. Also the structure of the hydrate derivative {[AgCI(TPTP)(3)] . (0.5 . H(2)O)} (2) of the corresponding known
Adeline M Hajjar et al.
Infection and immunity, 74(12), 6730-6738 (2006-09-20)
Francisella tularensis is an intracellular gram-negative bacterium that is highly infectious and potentially lethal. Several subspecies exist of varying pathogenicity. Infection by only a few organisms is sufficient to cause disease depending on the model system. Lipopolysaccharide (LPS) of gram-negative
Chen Chen et al.
Biotechnology for biofuels, 11, 155-155 (2018-07-12)
Polysaccharide monooxygenases (PMOs) of the auxiliary activity 9 (AA9) family have been reported to oxidize C1, C4, and C6 positions in cellulose. However, currently no direct evidence exists that PMOs oxidize C6 positions in cellulose, and molecular mechanism of C1, C4
Li-Av Segev-Zarko et al.
Biochemistry, 57(13), 2024-2034 (2018-03-09)
Multidrug resistant bacteria possess various mechanisms that can sense environmental stresses such as antibiotics and antimicrobial peptides and rapidly respond to defend themselves. Two known defense strategies are biofilm formation and lipopolysaccharide (LPS) modification. Though LPS modifications are observed in

Protocolos

Explore mass spectrometry analysis of glycans for glycomic & glycoproteomic neutral & acidic glycan analysis. See a general mass spec glycan analysis procedure.

Explore mass spectrometry analysis of glycans for glycomic & glycoproteomic neutral & acidic glycan analysis. See a general mass spec glycan analysis procedure.

Explore mass spectrometry analysis of glycans for glycomic & glycoproteomic neutral & acidic glycan analysis. See a general mass spec glycan analysis procedure.

Explore mass spectrometry analysis of glycans for glycomic & glycoproteomic neutral & acidic glycan analysis. See a general mass spec glycan analysis procedure.

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