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2-Cyanophenothiazine, 98%|453322|38642-74-9

2-Cyanophenothiazine, 98%

Cat. No JK453322_5_G
J&K Chemical

Product Information

Product Name
2-Cyanophenothiazine, 98%
Brand Name
J&K
Product Number
453322
CAS
38642-74-9
Molecular Formula
C13H8N2S
Molecular Weight
224.28
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
  • 10H-Phenothiazine-2-carbonitrile
  • Phenothiazine-2-carbonitrile
PubChem CID
98841
IUPAC Name
10H-phenothiazine-2-carbonitrile
InChI Key
XZSIGWOVDPSPMG-UHFFFAOYSA-N
SMILES
C1=CC=C2C(=C1)NC3=C(S2)C=CC(=C3)C#N

Properties

Melting Point
203-207

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H302
H312
H332
H315
H319
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P301+P317
P302+P352
P362+P364
P304+P340
P332+P317
P264+P265
P305+P351+P338
P337+P317

References Data Source From Pubchem

Synthesis of New Phenothiazine Derivatives Bearing Triphenylphosphonium and F16 Cationic Groups in the 2-Alkyl Side Chain: Evaluation of Anticancer Activity and Mitochondrial Tropic Effects
Publication Name: Russian Journal of Bioorganic Chemistry
Publication Date: 2025-12
DOI: 10.1134/s1068162025603301

Efficient and Practical Synthesis of a Novel Lipophilic Phenothiazine Derivative with an α-Tocopherol Isoprenoid Side Chain
Publication Name: Russian Journal of General Chemistry
Publication Date: 2025-06
DOI: 10.1134/s1070363225601826

2-Aminomethyl phenothiazine, its alkyl and triphenylphosphonium derivatives suppress erastin-induced ferroptosis in BT-474 cells but exhibit distinct cytotoxic activities
Publication Name: Naunyn-Schmiedeberg's Archives of Pharmacology
Publication Date: 2025-03-05
DOI: 10.1007/s00210-025-03986-3

Merging Chemical Techniques with CDC
Publication Name: Science of Synthesis
Publication Date: 2023

Visible-Light-Mediated C—N Bond Formation via Cross-Dehydrogenative Radical-Radical Reactions
Publication Name: Science of Synthesis
Publication Date: 2023

2-Cyanophenothiazine, 98%

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