461009-52-9

Basic information

• Product Name: 1,4-dichloro-1,4-diphenyl-2,3-diaza-1,3-butadiene
• Synonyms: 1,4-dichloro-1,4-diphenyl-2,3-diaza-1,3-butadiene
• CAS NO: 461009-52-9
• Molecular Weight: 277.153
• Mol File: 461009-52-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,4-dichloro-1,4-diphenyl-2,3-diaza-1,3-butadiene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-dichloro-1,4-diphenyl-2,3-diaza-1,3-butadiene(461009-52-9)
• EPA Substance Registry System: 1,4-dichloro-1,4-diphenyl-2,3-diaza-1,3-butadiene(461009-52-9)

Safety Data

• Hazardous Substances Data: 461009-52-9(Hazardous Substances Data)

Upstream product

• 28867-76-7 benzaldehyde benzylidenehydrazone 
• 98-88-4 benzoyl chloride 
• 613-94-5 benzoic acid hydrazide 
• 787-84-8 N'-benzoylbenzohydrazide 
• 4460-46-2 3-chloro-3-phenyl-3H-diazirine 
• 109-66-0 pentane 
• 865-49-6 chloroform-d1 
• 1670-14-0 benzamidine monohydrochloride 

Downstream Products

• 37144-02-8 3,5-diphenyl-4-propyl-4H-[1,2,4]triazole 
• 140133-82-0 3,3'-dimethyl-5,5'-diphenyl-4,4'-bi-4H-1,2,4-triazole 
• 32675-51-7 4-ethyl-3,5-diphenyl-4H-1,2,4-triazole 
• 135643-55-9 bis(α-ethylaminobenzylidene)hydrazine 
• 135643-61-7 3,5-diphenyl-4-(2-propyl)-4H-1,2,4-triazole 
• 135643-56-0 bis(α-isopropylaminobenzylidene)hydrazine 
• 28193-90-0 4-benzyl-3,5-diphenyl-4H-1,2,4-triazole 
• 1329449-22-0 4-(2,6-dimethylphenyl)-3,5-diphenyl-4H-1,2,4-triazole 
• 29091-56-3 4-(4-bromophenyl)-3,5-diphenyl-4H-1,2,4-triazole 
• 2039-06-7 3,5-diphenyl-1,2,4-triazole 
• 193685-14-2 4-allyl-3,5-diphenyl-4H-1,2,4-triazole 
• 135643-66-2 bis(α-methylaminobenzylidene)hydrazine 
• 32272-86-9 3,5-diphenyl-4-methyl-1,2,4-4H-triazole 
• 135643-58-2 bis(α-tert-butylaminobenzylidene)hydrazine 

Relevant articles and documents

ORGANOMETALLIC COMPLEX AND LIGHT-EMITTING ELEMENT, LIGHTING DEVICE, AND ELECTRONIC DEVICE INCLUDING THE ORGANOMETALLIC COMPLEX

A first object is to provide an organometallic complex capable of exhibiting phosphorescence. In General Formula (G1), at least one substituent of R11 to R14 represents any of a halogen group, a haloalkyl group having 1 to 4 carbon atoms, and a cyano group. At least one substituent of R15 to R19 represents any of a halogen group, a haloalkyl group having 1 to 4 carbon atoms, and a cyano group. R20 represents any of an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 5 to 8 carbon atoms, an aryl group having 6 to 12 carbon atoms, and a heteroaryl group having 4 to 10 carbon atoms. M is either a Group 9 element or a Group 10 element. When M is a Group 9 element, n is 3, and when M is a Group 10 element, n is 2.

Triazole Derivative, Light-Emitting Element, Light-Emitting Device, and Electronic Device

A substance having high excitation energy is provided. In particular, a substance having high triplet excitation energy is provided. Further, a light-emitting element, a light-emitting device, and an electronic device each having high emission efficiency and low driving voltage are provided. A triazole derivative to which an amino group is bonded is provided. In addition, a light-emitting element, a light-emitting device, and an electronic device each including the triazole derivative to which the amino group is bonded are provided.

Inter- and innermolecular reactions of chloro(phenyl)carbene

Supramolecular photolyses of 3-chloro-3-phenyl-3H-diazirine (8) were performed within cyclodextrin (CyD) hosts to determine whether these toroidal inclusion compounds could alter the reactivity of the ensuing carbene reaction intermediate, chloro(phenyl)carbene (9). Remarkably, no intramolecular products stemming from carbene 9 could be detected. Instead, modified CyDs were formed via so-called innermolecular reactions. Hence, diazirine 8 was photolyzed in various conventional solvents to gauge the intermolecular reactivity of carbene 9. Relevant results were used to rationalize the CyD innermolecular reaction products.