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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)-

Pyrrolo[3,4-c]pyrrole-1,3(2H,3aH)-dione, tetrahydro-2-(phenylmethyl)-

O=C1C2CNCC2C(=O)N1Cc1ccccc1 Request for Quotation
Chemical Name: Pyrrolo[3,4-c]pyrrole-1,3(2H,3aH)-dione, tetrahydro-2-(phenylmethyl)-
CAS Number: 86732-32-3
Product Number: AG003GLL(AGN-PC-00K9BW)
Synonyms:
MDL No: MFCD09037855
Molecular Formula: C13H14N2O2
Molecular Weight: 230.2625

Identification/Properties

Properties
BP:
459.941 °C at 760 mmHg
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
230.267g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
230.106g/mol
Monoisotopic Mass:
230.106g/mol
Topological Polar Surface Area:
49.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
314
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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-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


2-Benzyl-tetrahydro-pyrrolo[3,4-c]pyrrole-1,3-dione is a versatile compound used in chemical synthesis for its unique reactivity and structural characteristics. It serves as a valuable building block in the formation of various organic compounds through several key applications.One of the primary uses of 2-Benzyl-tetrahydro-pyrrolo[3,4-c]pyrrole-1,3-dione is as a starting material for the synthesis of complex natural products and pharmaceuticals. Its cyclic structure and reactive functional groups make it an ideal precursor for the creation of diverse molecular structures with specific biological activities and properties.Additionally, this compound is employed in the development of novel materials and polymers. By incorporating 2-Benzyl-tetrahydro-pyrrolo[3,4-c]pyrrole-1,3-dione into polymerization reactions, researchers can tailor the physical and chemical properties of resulting materials, leading to advanced applications in various industries such as electronics, coatings, and adhesives.Furthermore, 2-Benzyl-tetrahydro-pyrrolo[3,4-c]pyrrole-1,3-dione plays a crucial role in the construction of molecular frameworks for academic research purposes. Its structure can be modified and functionalized to create diverse chemical libraries, enabling the exploration of new reactions and methodologies in organic chemistry.Overall, the application of 2-Benzyl-tetrahydro-pyrrolo[3,4-c]pyrrole-1,3-dione in chemical synthesis extends across multiple disciplines, providing chemists with a versatile tool for the design and preparation of intricate molecules and materials.