1. Home
  2. 2,5-Piperazinedione, 3,6-bis[(aminooxy)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)-

2,5-Piperazinedione, 3,6-bis[(aminooxy)methyl]-

NOCC1NC(=O)C(NC1=O)CON Request for Quotation
Chemical Name: 2,5-Piperazinedione, 3,6-bis[(aminooxy)methyl]-
CAS Number: 1204-99-5
Product Number: AG00268P(AGN-PC-0JLUV7)
Synonyms:
MDL No:
Molecular Formula: C6H12N4O4
Molecular Weight: 204.1839

Identification/Properties

Computed Properties
Molecular Weight:
204.186g/mol
XLogP3:
-3
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
204.086g/mol
Monoisotopic Mass:
204.086g/mol
Topological Polar Surface Area:
129A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
210
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
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


2,5-Piperazinedione, 3,6-bis[(aminooxy)methyl]- is a versatile compound widely used in chemical synthesis for its exceptional properties. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for efficient binding with a wide range of functional groups, making it an indispensable tool for organic chemists looking to create complex molecular structures. By incorporating 2,5-Piperazinedione, 3,6-bis[(aminooxy)methyl]- into their synthetic pathways, researchers can achieve precise control over the formation of crucial chemical bonds, enabling the development of novel compounds with tailored properties and diverse applications in industries such as medicine, agriculture, and materials science.