1. Home
  2. 1,7-bis(bromomethyl)-2,6-dimethylpyrazolo[1,2-a]pyrazole-3,5-dione

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)-

1,7-bis(bromomethyl)-2,6-dimethylpyrazolo[1,2-a]pyrazole-3,5-dione

BrCc1c(C)c(=O)n2n1c(CBr)c(c2=O)C Request for Quotation
Chemical Name: 1,7-bis(bromomethyl)-2,6-dimethylpyrazolo[1,2-a]pyrazole-3,5-dione
CAS Number: 68654-25-1
Product Number: AG00FABY(AGN-PC-0JMK9P)
Synonyms:
MDL No: MFCD00036952
Molecular Formula: C10H10Br2N2O2
Molecular Weight: 350.0066

Identification/Properties

Computed Properties
Molecular Weight:
350.01g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
349.909g/mol
Monoisotopic Mass:
347.911g/mol
Topological Polar Surface Area:
40.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
414
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Dibromobimane, also known as DBB, is a versatile chemical compound widely utilized in chemical synthesis for various applications. With its unique properties, Dibromobimane acts as a potent reagent in the modification and labeling of bioactive molecules, particularly sulfhydryl-containing compounds. This compound is proficient in selectively targeting and conjugating with thiol groups, aiding in the synthesis of tailored molecules for research and pharmaceutical development. Furthermore, Dibromobimane finds use in the creation of fluorescent probes and detection assays, contributing significantly to the advancement of biochemistry and molecular biology studies. Its ability to specifically react with thiol groups makes it a valuable tool in protein analysis and structural elucidation, showcasing its importance in a wide array of chemical synthesis processes.