1. Home
  2. 6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-3-carbaldehyde

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-3-carbaldehyde

O=Cc1cnc2n1CCC2 Request for Quotation
Chemical Name: 6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-3-carbaldehyde
CAS Number: 914637-04-0
Product Number: AG00GVXN(AGN-PC-00OUUL)
Synonyms:
MDL No:
Molecular Formula: C7H8N2O
Molecular Weight: 136.1512

Identification/Properties

Computed Properties
Molecular Weight:
136.154g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
136.064g/mol
Monoisotopic Mass:
136.064g/mol
Topological Polar Surface Area:
34.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
149
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

Request for Quotation

Customer Feedback

Chemical Structure


6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-3-carbaldehyde is a versatile compound commonly used in chemical synthesis for the preparation of various heterocyclic compounds. This aldehyde derivative serves as a key building block in the formation of complex organic molecules due to its unique structural properties and reactivity.In organic synthesis, 6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-3-carbaldehyde can undergo a variety of reactions such as nucleophilic addition, condensation, and cyclization. It can participate in multicomponent reactions to form fused heterocycles or act as a precursor for the introduction of functional groups.Furthermore, this compound is often utilized in the design and creation of bioactive molecules, pharmaceutical intermediates, and agrochemicals. Its ability to undergo diverse transformations makes it a valuable tool for medicinal chemistry research and the development of new drug candidates with potential therapeutic applications.