12H-Benzo[b]phenothiazine TCI B6562

Chemical Identity

CAS No.: 258-08-2
PubChem: CID 255516
Formula: C16H11NS
Molecular weight: 249.33 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 12H-benzo[b]phenothiazine
SMILES: C1=CC=C2C=C3C(=CC2=C1)NC4=CC=CC=C4S3
InChIKey: IWKDFAWZFVGWAH-UHFFFAOYSA-N
MDL: MDL00823535

Rp 1.298.850,00

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Berat 1g 5g

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TCI B6562 is 12H-benzo[b]phenothiazine, an extended phenothiazine scaffold in which an additional benzene ring is fused onto the classic sulfur- and nitrogen-bridged tricyclic core. Phenothiazine derivatives are well known as strong electron donors and as foundational structures in dye chemistry, and the extended conjugation here shifts their optical behaviour. The free N–H position offers a convenient handle for alkylation or arylation, allowing solubility and electronic properties to be tuned. AMI Scientific supplies this TCI product in 1 g and 5 g pack sizes; consult the official TCI documentation and safety data sheet before use.

TCI brochures (PDF)

Visible Light Photoredox Organocatalyst for Carbon (sp3)-Heteroatom Bond Formation 2026-09-10 · p. 1

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Shahrisa et al. (2015). Chemoselective Sequential Reactions for the Synthesis of 12H-Benzo[a]xanthenes and Dihydro-1H-naphtho[1,2-e][1,3]oxazines. Synlett doi:10.1055/s-0034-1380323
Tandon et al. (2009). 2,3-Disubstituted-1,4-naphthoquinones, 12H-benzo[b]phenothiazine-6,11-diones and related compounds: Synthesis and Biological evaluation as potential antiproliferative and antifungal agents. European Journal of Medicinal Chemistry doi:10.1016/j.ejmech.2008.06.025
Ektova et al. (1993). A Smiles Rearrangement as an Intermediate Step in the Formation of 8-Bromo-7-hydroxy-N-(4’ -N,N-diethylaminophenyl)-12H-benzo[b]phenothiazine-6,11-quinone 6-lmine from 2-(2’ -Aminophenylthio)-6-bromo-5-hydroxy-N-(4-/V,/V-diethylaminophenyl)-1,4-naphthoquinone 4-lmine. Mendeleev Communications doi:10.1070/mc1993v003n01abeh000205

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.