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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)-

1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole;dihydrochloride

N1Cc2c(C1)cn[nH]2.Cl.Cl Request for Quotation
Chemical Name: 1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole;dihydrochloride
CAS Number: 157327-47-4
Product Number: AG001PDI(AGN-PC-07YNFW)
Synonyms:
MDL No:
Molecular Formula: C5H9Cl2N3
Molecular Weight: 182.0511

Identification/Properties

Computed Properties
Molecular Weight:
182.048g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
181.017g/mol
Monoisotopic Mass:
181.017g/mol
Topological Polar Surface Area:
40.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
93.7
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:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4,5,6-Tetrahydropyrrolo[3,4-c]pyrazole dihydrochloride is a versatile chemical compound widely utilized in chemical synthesis processes. Due to its unique molecular structure and reactivity, this compound serves as a valuable building block in the creation of various organic molecules. In chemical synthesis, it acts as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its presence in the reaction mixture facilitates the formation of complex molecular structures through controlled transformations, enabling chemists to access novel compounds with potential applications in medicinal chemistry, material science, and other fields.