Cas no 945217-56-1 (3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole)

3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole structure
945217-56-1 structure
Product Name:3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole
CAS No:945217-56-1
MF:C6H9N3
MW:123.155760526657
MDL:MFCD16658458
CID:823608
PubChem ID:55287365
Update Time:2024-10-25

3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Chemical and Physical Properties

Names and Identifiers

    • 3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole
    • 1,4,5,6-tetrahydro-3-methyl-Pyrrolo[3,4-c]pyrazole
    • 3-Methyl-1,4,5,6-tetrahydro-pyrrolo[3,4-c]pyrazole
    • 3-methyl-2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole
    • 1,4,5,6-Tetrahydro-3-methylpyrrolo[3,4-c]pyrazole (ACI)
    • 3-Methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole
    • 945217-56-1
    • VMB21756
    • CS-0053873
    • MFCD16658458
    • DA-19474
    • SCHEMBL1705256
    • SCHEMBL17162823
    • DTXSID10717495
    • PB18158
    • AKOS006356870
    • 3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole
    • MDL: MFCD16658458
    • Inchi: 1S/C6H9N3/c1-4-5-2-7-3-6(5)9-8-4/h7H,2-3H2,1H3,(H,8,9)
    • InChI Key: BRIYFUKTRQTBLR-UHFFFAOYSA-N
    • SMILES: N1=C(C)C2CNCC=2N1

Computed Properties

  • Exact Mass: 123.079647300g/mol
  • Monoisotopic Mass: 123.079647300g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 0
  • Complexity: 115
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.4
  • Topological Polar Surface Area: 40.7?2

3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Pricemore >>

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3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Water ;  1.5 h, rt
Reference
Preparation of phenylheteroarylpiperidinamine derivatives for use as dipeptidyl peptidase-IV inhibitors
, World Intellectual Property Organization, , ,

Production Method 2

Reaction Conditions
Reference
Heterocyclic compounds as dipeptidyl peptidase-iv inhibitors for the treatment or prevention of diabetes
, United States, , ,

Production Method 3

Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Ethanol ,  Water ;  3 h, 90 °C
Reference
Preparation of substituted six-membered heterocyclic amine compounds as DPP-IV inhibitors
, China, , ,

Production Method 4

Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Methanol ;  12 h, rt
1.2 Reagents: Ammonium hydroxide ,  Ammonia Solvents: Methanol ,  Water
Reference
Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes, hyperglycemia, and obesity
, United States, , ,

Production Method 5

Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Water ;  1.5 h, rt
Reference
Preparation of pyrrolopyrazolylaminocyclohexanes and related compounds as dipeptidylpeptidase-IV (DPP-IV) inhibitors for the treatment or prevention of diabetes
, World Intellectual Property Organization, , ,

3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Raw materials

3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Preparation Products

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