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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-Propenoic Acid,3(5-Nitro-1-Cyclohexen-1-Yl)-(2E)

OC(=O)/C=C/C1=CCCC(C1)[N+](=O)[O-] Request for Quotation
Chemical Name: 2-Propenoic Acid,3(5-Nitro-1-Cyclohexen-1-Yl)-(2E)
CAS Number: 899809-64-4
Product Number: AG00GUIM(AGN-PC-0WAG6G)
Synonyms:
MDL No:
Molecular Formula: C9H11NO4
Molecular Weight: 197.1879

Identification/Properties

Computed Properties
Molecular Weight:
197.19g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
197.069g/mol
Monoisotopic Mass:
197.069g/mol
Topological Polar Surface Area:
83.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
300
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
1
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-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(E)-3-(5-Nitrocyclohex-1-en-1-yl)acrylic acid is a versatile compound that finds wide applications in chemical synthesis. Due to its unique structure and reactive properties, it serves as a valuable building block in the creation of various organic compounds. One prominent application of this compound is in the synthesis of specialized polymer materials. Its incorporation into polymer chains can impart specific desired characteristics such as improved flexibility, thermal stability, or adhesion properties. Additionally, (E)-3-(5-Nitrocyclohex-1-en-1-yl)acrylic acid can be utilized in the preparation of advanced pharmaceutical intermediates, where its chemical reactivity plays a crucial role in forming key molecular structures. Furthermore, its involvement in the development of novel organic frameworks for materials science and catalysis showcases its significance in driving innovation within the field of chemistry. By harnessing the capabilities of (E)-3-(5-Nitrocyclohex-1-en-1-yl)acrylic acid, researchers and chemists can explore new avenues for creating high-performance materials and compounds with tailored properties.