Benzalazine

Base Information

• Chemical Name: Benzalazine
• CAS No.: 28867-76-7
• Molecular Formula: C14H12 N2
• Molecular Weight: 208.263
• Hs Code.: 2928000090
• European Community (EC) Number: 209-627-6,631-102-9
• NSC Number: 3269
• UNII: G68LHD5XNY
• ChEMBL ID: CHEMBL3199194
• Mol file: 28867-76-7.mol

Synonyms:benzalazine

Chemical Property of Benzalazine

Chemical Property:

• Vapor Pressure: 0.000681mmHg at 25°C
• Melting Point: 92-93 °C(lit.)
• Refractive Index: 1.6152 (estimate)
• Boiling Point: 318.3°Cat760mmHg
• Flash Point: 138.3°C
• PSA: 24.72000
• Density: 0.98g/cm³
• LogP: 3.13960
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 208.100048391
• Heavy Atom Count: 16
• Complexity: 207

Purity/Quality:

99% ^*data from raw suppliers

Benzalazine ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Nitrogen Compounds -> Hydrazines
• Canonical SMILES: C1=CC=C(C=C1)C=NN=CC2=CC=CC=C2
• Isomeric SMILES: C1=CC=C(C=C1)/C=N/N=C/C2=CC=CC=C2

Technology Process of Benzalazine

There total 160 articles about Benzalazine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 76.0%

benzylhydrazine oxalate (32064-65-6) → benzaldehyde (100-52-7) + toluene (108-88-3,15644-74-3,16713-13-6) + benzaldehyde benzylidenehydrazone (28867-76-7)

Guidance literature:

With tetrachloromethane; ammonium hydroxide; for 96h; Ambient temperature;

Reference yield: 60.0%

benzil dihydrazone (4702-78-7) → phenyl benzyl ketone (451-40-1) + lophine (484-47-9) + benzaldehyde benzylidenehydrazone (28867-76-7)

Guidance literature:

at 180 ℃;

DOI:10.1002/ejoc.200700848

Reference yield: 40.0%

phenyldiazomethane (908094-04-2) + benzaldehyde (100-52-7) → phenyl benzyl ketone (451-40-1) + (E)-1,2-diphenyl-ethene (103-30-0) + benzaldehyde benzylidenehydrazone (28867-76-7)

Guidance literature:

zinc(II) iodide; In diethyl ether; for 2h; Ambient temperature;

upstream raw materials:

3-methyl-4,5-dihydro-6-oxopyridazine

benzaldehyde

phenyldiazomethane

{Ta(O-2,6-C6H3-i-Pr2)3(THF)}2(μ-N2)

Downstream raw materials:

4,8-Diphenyl-octahydro-2,6-dithia-3b,7b-diaza-dicyclopenta[a,e]pentalene 2,2,6,6-tetraoxide

benzylidene-[2-phenyl-4-(2,2,2-trifluoro-1-trifluoromethyl-ethylidene)-[1,3]thiazetidin-3-yl]-amine

Ta(NNCHPh)(S-2,4,6-C₆H₂-i-Pr₃)3(THF)

Ta(NNCHPh)(O-2,6-C₆H₃-i-Pr₂)3(THF)

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