1. Home
  2. 7H-Furo[3,2-g][1]benzopyran-7-one,4-[[(2E)-3,7-dimethyl-2,6-octadienyl]oxy]-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

7H-Furo[3,2-g][1]benzopyran-7-one,4-[[(2E)-3,7-dimethyl-2,6-octadienyl]oxy]-

CC(=CCOc1c2ccoc2cc2c1ccc(=O)o2)CCC=C(C)C Request for Quotation
Chemical Name: 7H-Furo[3,2-g][1]benzopyran-7-one,4-[[(2E)-3,7-dimethyl-2,6-octadienyl]oxy]-
CAS Number: 7380-40-7
Product Number: AG005KHO(AGN-PC-0U3Z1K)
Synonyms:
MDL No:
Molecular Formula: C21H22O4
Molecular Weight: 338.3970

Identification/Properties

Properties
MP:
51-54°C
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
338.403g/mol
XLogP3:
5.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
338.152g/mol
Monoisotopic Mass:
338.152g/mol
Topological Polar Surface Area:
48.7A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
570
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Bergaptin, also known as 5-Methoxypsoralen, is a natural compound commonly found in certain plants such as bergamot oranges. In chemical synthesis, Bergaptin is a versatile molecule that is utilized for its unique photochemical properties. One key application of Bergaptin in chemical synthesis is its use as a psoralen derivative in DNA interstrand crosslinking studies. Psoralens are compounds that exhibit photoreactivity, meaning they can form covalent bonds with nucleic acids when activated by ultraviolet (UV) light. This property makes Bergaptin an important tool in DNA research and the development of novel therapeutic agents for diseases such as cancer.Furthermore, Bergaptin can also be employed as a photoactivatable crosslinking agent in protein-protein interaction studies. By tethering proteins with Bergaptin derivatives and using UV light to induce crosslinking, researchers can probe complex protein structures and understand intricate biological pathways.Overall, Bergaptin plays a crucial role in advancing chemical synthesis techniques, particularly in the fields of DNA and protein research. Its photochemical properties and reactivity make it a valuable compound for studying molecular interactions and developing new strategies for drug discovery and therapeutic applications.