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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)-

5-octylthieno[3,4-c]pyrrole-4,6-dione

CCCCCCCCN1C(=O)c2c(C1=O)csc2 Request for Quotation
Chemical Name: 5-octylthieno[3,4-c]pyrrole-4,6-dione
CAS Number: 773881-43-9
Product Number: AG00G50I(AGN-PC-0HF2Q6)
Synonyms:
MDL No:
Molecular Formula: C14H19NO2S
Molecular Weight: 265.3712

Identification/Properties

Computed Properties
Molecular Weight:
265.371g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
7
Exact Mass:
265.114g/mol
Monoisotopic Mass:
265.114g/mol
Topological Polar Surface Area:
65.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
297
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:
H315-H319-H335-H412
Precautionary Statements:
P261-P273-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Octyl-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block for designing and creating various organic molecules with unique properties and functions. In chemical synthesis, $name$ is often employed as a precursor in the synthesis of organic semiconductors, polymers, and materials for optoelectronic applications. Its structural features make it a valuable intermediate for introducing functional groups and modulating the electronic properties of the final products. Additionally, $name$ exhibits excellent stability and compatibility with a wide range of synthetic methodologies, making it a preferred choice for researchers and chemists working in the field of organic synthesis.