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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)-

tert-butyl 3-(hydrazinecarbonyl)azetidine-1-carboxylate

NNC(=O)C1CN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 3-(hydrazinecarbonyl)azetidine-1-carboxylate
CAS Number: 1001907-44-3
Product Number: AG00016N(AGN-PC-07YK8X)
Synonyms:
MDL No:
Molecular Formula: C9H17N3O3
Molecular Weight: 215.2496

Identification/Properties

Computed Properties
Molecular Weight:
215.253g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
215.127g/mol
Monoisotopic Mass:
215.127g/mol
Topological Polar Surface Area:
84.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
266
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 3-(hydrazinecarbonyl)azetidine-1-carboxylate is a versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it a valuable building block for the preparation of various organic compounds. In chemical synthesis, this compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It can undergo numerous transformations, such as nucleophilic addition reactions, to introduce specific functional groups into the target molecules. Additionally, tert-Butyl 3-(hydrazinecarbonyl)azetidine-1-carboxylate can be utilized in the development of novel materials and bioactive compounds with potential applications in drug discovery and materials science.