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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)-

2-(1-(Ethylsulfonyl)azetidin-3-ylidene)acetonitrile

CCS(=O)(=O)N1CC(=CC#N)C1 Request for Quotation
Chemical Name: 2-(1-(Ethylsulfonyl)azetidin-3-ylidene)acetonitrile
CAS Number: 1187595-85-2
Product Number: AG008RKE(AGN-PC-0WANI9)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O2S
Molecular Weight: 186.2315

Identification/Properties

Computed Properties
Molecular Weight:
186.229g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
186.046g/mol
Monoisotopic Mass:
186.046g/mol
Topological Polar Surface Area:
69.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
333
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(1-(Ethylsulfonyl)azetidin-3-ylidene)acetonitrile is a versatile compound widely utilized in chemical synthesis for its unique properties. This compound serves as an important building block in the development of various organic molecules with diverse applications. In particular, it is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals due to its ability to introduce specific functional groups into target molecules. Additionally, the presence of the ethylsulfonyl and acetonitrile groups in this compound enables it to participate in a range of traditional organic reactions, such as nucleophilic substitutions and addition reactions, leading to the formation of complex molecular structures. Furthermore, the azetidin-3-ylidene moiety imparts steric and electronic effects that can influence the reactivity and selectivity of the compound in chemical transformations. Overall, 2-(1-(Ethylsulfonyl)azetidin-3-ylidene)acetonitrile plays a crucial role in the synthesis of valuable compounds in the field of organic chemistry.