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  2. (R)-5-ALLYL-2-OXABICYCLO[3.3.0]OCT-8-ENE

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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)-

(R)-5-ALLYL-2-OXABICYCLO[3.3.0]OCT-8-ENE

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Chemical Name: (R)-5-ALLYL-2-OXABICYCLO[3.3.0]OCT-8-ENE
CAS Number: 911200-98-1
Product Number: AG003CAJ(AGN-PC-0WAKCN)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
Form:
Liquid
Computed Properties
Molecular Weight:
150.221g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
150.104g/mol
Monoisotopic Mass:
150.104g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
205
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-5-Allyl-2-oxabicyclo[3.3.0]oct-8-ene, 95% is a versatile and valuable compound in chemical synthesis. This compound is widely utilized as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and high purity make it a preferred choice for synthetic chemists looking to access complex molecules efficiently and selectively. By incorporating (R)-5-Allyl-2-oxabicyclo[3.3.0]oct-8-ene, 95% into their reactions, researchers can introduce allyl and oxabicyclic functionalities with high stereocontrol, enabling the synthesis of intricate molecular frameworks with enhanced synthetic efficiency and atom economy.