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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)-

Hydrazinecarboxylic acid, (phenylmethylene)-, 1,1-dimethylethyl ester

O=C(OC(C)(C)C)NN=Cc1ccccc1 Request for Quotation
Chemical Name: Hydrazinecarboxylic acid, (phenylmethylene)-, 1,1-dimethylethyl ester
CAS Number: 24469-50-9
Product Number: AG002O8F(AGN-PC-0JUZBX)
Synonyms:
MDL No:
Molecular Formula: C12H16N2O2
Molecular Weight: 220.2676

Identification/Properties

Computed Properties
Molecular Weight:
220.272g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
220.121g/mol
Monoisotopic Mass:
220.121g/mol
Topological Polar Surface Area:
50.7A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
250
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (E)-tert-Butyl 2-benzylidenehydrazinecarboxylate is a versatile compound commonly utilized in chemical synthesis applications. With its unique structure and reactivity, this compound serves as a valuable building block for the creation of various organic molecules. In particular, (E)-tert-Butyl 2-benzylidenehydrazinecarboxylate is often employed as a key intermediate in the synthesis of complex organic compounds, such as pharmaceuticals and agrochemicals.Due to its ability to undergo diverse chemical transformations, this compound can be utilized in the development of novel compounds with desirable properties. (E)-tert-Butyl 2-benzylidenehydrazinecarboxylate plays a crucial role in the formation of carbon-carbon and carbon-nitrogen bonds, enabling the synthesis of structurally intricate molecules. Additionally, its stereochemistry can be leveraged to control the regioselectivity and stereoselectivity of reactions, leading to the production of specific enantiomers or diastereomers.In summary, the application of (E)-tert-Butyl 2-benzylidenehydrazinecarboxylate in chemical synthesis offers chemists a valuable tool for building complex organic molecules with precision and efficiency.