4616-17-5

Basic information

• Product Name: Acetaldehyde, (3-methyl-2(3H)-benzothiazolylidene)-
• CAS NO: 4616-17-5
• Molecular Formula: C10H9NOS
• Molecular Weight: 191.254
• Mol File: 4616-17-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetaldehyde, (3-methyl-2(3H)-benzothiazolylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetaldehyde, (3-methyl-2(3H)-benzothiazolylidene)-(4616-17-5)
• EPA Substance Registry System: Acetaldehyde, (3-methyl-2(3H)-benzothiazolylidene)-(4616-17-5)

Safety Data

• Hazardous Substances Data: 4616-17-5(Hazardous Substances Data)

Upstream product

• 2786-41-6 2-<(2,3-Dihydro-3-methylbenzothiazol-2-yliden)methyl>-2,3-dihydro-3-methylbenzothiazol 

Downstream Products

• 127868-36-4 2-[(E)-4-(2,6-Diphenyl-pyran-4-ylidene)-but-2-en-(E)-ylidene]-3-methyl-2,3-dihydro-benzothiazole 
• 75558-43-9 2-[2-(2,6-Diphenyl-pyran-4-ylidene)-eth-(Z)-ylidene]-3-methyl-2,3-dihydro-benzothiazole 
• 1332702-69-8 C₂₆H₂₅BF₂N₂O₂S 
• 13636-81-2 {4-[2-(3-methyl-3H-benzothiazol-2-ylidene)-ethylidene]-5-oxo-[1,3]dithiolan-2-ylidene}-phenyl-acetonitrile 

Relevant articles and documents

Heterocyclic 8?-Systems, 14. Generation and Reactions of Cyanine Dye Leuko compounds.

The symmetric cyanine dyes 2a - c, 3a, 4a, and 5a were transformed into the leuko compounds 7 - 10, 12, and 14.Deprotonation of 7 and 8 with lithium diisopropylamide led to the corresponding cyanine dye anions, which yielded derivatives of the leuko compounds (25 - 30 and 34, 35, respectively) with electrophiles.The cyanine dyes 2a, 3a and the leuko compounds 7, 8 delivered with lithium tetracyano-p-quinodimethan anion (LiTCNQ) and tetracyano-p-quinodimethan (TCNQ) simple (36, 37) and complex salts (38, 39), respectively. 39 displayed interesting conductivity.