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2-(4-Bromophenyl)benzothiazole, 99.9%|285614|19654-19-4

2-(4-Bromophenyl)benzothiazole, 99.9%

Cat. No JK285614_25_G
J&K Chemical

Product Information

Product Name
2-(4-Bromophenyl)benzothiazole, 99.9%
Brand Name
J&K
Product Number
285614
CAS
19654-19-4
Molecular Formula
C13H8BrNS
Molecular Weight
290.18
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2320602
IUPAC Name
2-(4-bromophenyl)-1,3-benzothiazole
InChI Key
FQIRBKKYMJKENC-UHFFFAOYSA-N
SMILES
C1=CC=C2C(=C1)N=C(S2)C3=CC=C(C=C3)Br

Properties

Density
1.545
Melting Point
132.0 - 135.0

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Danger
Hazard Statement
H302
H315
H319
H335
H336
Precautionary Statement
P264
P270
P330
P280
P261
P271
P405
P319
P301+P317
P302+P352
P332+P317
P305+P351+P338
P264+P265
P337+P317
P304+P340
P403+P233
Storage Condition
Room temperature

References Data Source From Pubchem

An ecofriendly and efficient approach for three-component synthesis of benzothiazoles: research on catalytic application of Fe3O4@DOP-Amide/Imid-CuCl2 nanocomposite
Publication Name: Research on Chemical Intermediates
Publication Date: 2024-07-20
DOI: 10.1007/s11164-024-05347-w

Reactions of α-Phenylglyoxylic Acids with ortho-Functionalized Anilines in Deep Eutectic Solvents: Selective Syntheses of 3-Aryl-2H-benzo[b][1,4]oxazin-2-ones, 2-Arylbenzothiazoles, and 3-Arylquinoxalin-2(1H)-ones
Publication Name: Synthesis
Publication Date: 2022-03-17
DOI: 10.1055/a-1780-1691

Synthesis of 2-Arylbenzothiazoles from Nitrobenzenes, Benzylamines, and Elemental Sulfur via Redox Cyclization
Publication Name: Synlett
Publication Date: 2022-01-18
DOI: 10.1055/s-0041-1737760

Photoredox- and Nickel-Catalyzed Phosphonylation of Aryl Halides
Publication Name: Synfacts
Publication Date: 2021-02-16
DOI: 10.1055/s-0040-1706710

Current advances in the synthetic strategies of 2-arylbenzothiazole
Publication Name: Molecular Diversity
Publication Date: 2020-11-12
DOI: 10.1007/s11030-020-10149-4

2-(4-Bromophenyl)benzothiazole, 99.9%

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