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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)-

3-Azetidinecarbonitrile, 1-(phenylmethyl)-

N#CC1CN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: 3-Azetidinecarbonitrile, 1-(phenylmethyl)-
CAS Number: 94985-26-9
Product Number: AG006QFD(AGN-PC-02KH2G)
Synonyms:
MDL No:
Molecular Formula: C11H12N2
Molecular Weight: 172.2264

Identification/Properties

Properties
BP:
296.1 °C at 760 mmHg
Storage:
2-8℃;
Computed Properties
Molecular Weight:
172.231g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
172.1g/mol
Monoisotopic Mass:
172.1g/mol
Topological Polar Surface Area:
27A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
203
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


N-Benzyl-3-cyanoazetidine is a versatile compound commonly employed in organic synthesis for its unique reactivity and functional group compatibility. Its application in chemical synthesis lies in its ability to serve as a key intermediate in the preparation of various complex molecules. Due to its azetidine ring structure and cyano substituent, this compound participates in a variety of reactions, including nucleophilic additions, cyclizations, and cross-coupling reactions. In particular, N-Benzyl-3-cyanoazetidine is valued for its capacity to introduce the benzyl and cyano functional groups into target molecules, enabling the synthesis of diverse organic compounds with specific properties and biological activities. This compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials, making it a valuable building block in modern chemical synthesis.