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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzaldehyde, (phenylmethylene)hydrazone

c1ccc(cc1)C=NN=Cc1ccccc1 Request for Quotation
Chemical Name: Benzaldehyde, (phenylmethylene)hydrazone
CAS Number: 588-68-1
Product Number: AG003O0E(AGN-PC-0H889S)
Synonyms:
MDL No:
Molecular Formula: C14H12N2
Molecular Weight: 208.25848

Identification/Properties

Properties
MP:
92-94°C
BP:
318.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
208.264g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
208.1g/mol
Monoisotopic Mass:
208.1g/mol
Topological Polar Surface Area:
24.7A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
207
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H317-H319-H332-H335
Precautionary Statements:
P261-P264-P280-P305+P351+P338-P233
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzalazine, also known as 4-(phenylazo)benzaldehyde, is a versatile organic compound that finds widespread application in chemical synthesis. In the field of organic chemistry, Benzalazine serves as a key building block in the preparation of various azo compounds and a range of other functional materials.One of the primary uses of Benzalazine is in the synthesis of azo dyes, which are widely used in the textile industry for coloring fabrics. By reacting Benzalazine with other aromatic compounds containing amine groups, chemists can easily create vibrant and stable azo dyes that exhibit a wide range of hues.Furthermore, Benzalazine is also utilized in the preparation of pharmaceutical intermediates, particularly in the development of certain anti-inflammatory drugs and antioxidants. Its ability to undergo selective functional group transformations makes it a valuable tool for medicinal chemists seeking to modify the structure of bioactive compounds.In addition, Benzalazine can be employed in the synthesis of coordination complexes and metal-organic frameworks due to its ability to act as a bridging ligand. These complexes have applications in catalysis, sensing, and materials science, showcasing the diverse utility of Benzalazine in the realm of chemical synthesis.