1. Home
  2. 1-Propanamine, 3-(2-hydroxy-1-methyl-2-nitrosohydrazino)-N-methyl-

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)-

1-Propanamine, 3-(2-hydroxy-1-methyl-2-nitrosohydrazino)-N-methyl-

CN(N(N=O)O)CCCNC Request for Quotation
Chemical Name: 1-Propanamine, 3-(2-hydroxy-1-methyl-2-nitrosohydrazino)-N-methyl-
CAS Number: 146724-84-7
Product Number: AG001E9X(AGN-PC-0JK5UH)
Synonyms:
MDL No:
Molecular Formula: C5H14N4O2
Molecular Weight: 162.1903

Identification/Properties

Computed Properties
Molecular Weight:
162.193g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
162.112g/mol
Monoisotopic Mass:
162.112g/mol
Topological Polar Surface Area:
76.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
128
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-(2-Hydroxy-1-methyl-2-nitrosohydrazinyl)-N-methyl-1-propanamine serves as a versatile compound in chemical synthesis due to its unique structural features and reactive properties. Its hydroxyl, nitroso, and hydrazine groups allow for various functionalization reactions, making it a valuable intermediate in the preparation of diverse organic compounds. In particular, this compound can be utilized for the synthesis of specialized pharmaceuticals, agrochemicals, and complex organic molecules through coupling reactions, condensation reactions, and other transformative processes in organic chemistry. Its specific chemical properties enable precise control over the incorporation of functional groups, facilitating the synthesis of tailored molecules with desired properties and applications in a range of industrial and research settings.