Saltar al contenido
Merck
Todas las fotos(1)

Key Documents

View All Documentation

167576

Sigma-Aldrich

2-Chlorobenzothiazole

99%

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(1)

About This Item

Fórmula empírica (notación de Hill):
C7H4ClNS
Número de CAS:
615-20-3
Peso molecular:
169.63
Beilstein/REAXYS Number:
116316
EC Number:
210-415-0
MDL number:
MFCD00005776
UNSPSC Code:
12352100
PubChem Substance ID:
24850216
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.637 (lit.)

bp

141 °C/30 mmHg (lit.)

mp

21-23 °C (lit.)

density

1.303 g/mL at 25 °C (lit.)

SMILES string

Clc1nc2ccccc2s1

InChI

1S/C7H4ClNS/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4H

InChI key

BSQLQMLFTHJVKS-UHFFFAOYSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

Categorías relacionadas

Application

2-Chlorobenzothiazole was used in the synthesis of:
  • (RS)- and (S)-lubeluzole
  • (1,3-benzothiazol-2-yl) amino-9-(10H)-acridinone derivatives
  • 4H-thieno[2′,3′:4,5]pyrimido[2,1-b]benzothiazole derivatives

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Irrit. 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Florence Delmas et al.
European journal of medicinal chemistry, 39(8), 685-690 (2004-07-28)
(1,3-Benzothiazol-2-yl) amino-9-(10H)-acridinone derivatives were synthesized via a procedure based on the Ullman reaction and were assessed for their in vitro antileishmanial and anti-HIV activities. Two derivatives, 4-(6-nitro-benzothiazol-2-ylamino)-10H-acridin-9-one and 1-(6-amino-benzothiazol-2-ylamino)-10H-acridin-9-one, revealed a selective antileishmanial activity, mainly due to amastigote-specific toxicity. Results
Synthesis of new thienopyrimidobenzothiazoles and thienopyrimidobenzoxazoles with analgesic and antiinflammatory properties.
Russo F, et al.
European Journal of Medicinal Chemistry, 29(7), 569-578 (1994)
Damodara N Kommi et al.
Organic letters, 15(6), 1158-1161 (2013-02-26)
Three new, concise, and protecting group-free synthetic routes for (RS)- and (S)-lubeluzole are reported in higher (46-62%) overall yields compared to the reported procedures (6-35%). The key steps involve C-N bond formation via epoxide aminolysis and nucleophilic substitution of 2-chlorobenzothiazole
Anita K Kovács et al.
Frontiers in chemistry, 6, 120-120 (2018-05-05)
A general strategy for the synthesis of N-peptide-6-amino-D-luciferin conjugates has been developed. The applicability of the strategy was demonstrated with the preparation of a known substrate, N-Z-Asp-Glu-Val-Asp-6-amino-D-luciferin (N-Z-DEVD-aLuc). N-Z-DEVD-aLuc was obtained via a hybrid liquid/solid phase synthesis method, in which

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico