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2-endo-phenyl-2-exo-bicyclo<2.2.1>heptanediol is a complex organic compound with the molecular formula C13H16O2. It features a bicyclic structure with a phenyl group attached to the endo position of the first carbon atom and a hydroxyl group at the exo position of the second carbon atom. 2-endo-phenyl-2-exo-bicyclo<2.2.1>heptanediol is characterized by its unique stereochemistry, which arises from the fusion of two cyclohexane rings in a 2.2.1 pattern. The presence of both aromatic and hydroxyl functional groups makes it an interesting molecule for study in organic chemistry, potentially useful in the synthesis of various pharmaceuticals and other chemical products due to its ability to form hydrogen bonds and participate in π-π interactions.

1135-59-7

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1135-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1135-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1135-59:
(6*1)+(5*1)+(4*3)+(3*5)+(2*5)+(1*9)=57
57 % 10 = 7
So 1135-59-7 is a valid CAS Registry Number.

1135-59-7Relevant academic research and scientific papers

Antimalarial activity of novel 1,2,5,6-tetraoxacycloalkanes and 1,2,5-trioxacycloalkanes

Kim, Hye-Sook,Begum, Khurshida,Ogura, Naoki,Wataya, Yusuke,Nonami, Yuji,Ito, Toyonari,Masuyama, Araki,Nojima, Masatomo,McCullough, Kevin J.

, p. 1957 - 1961 (2003)

Photooxygenation of 2-phenylnorbornene 1 in the presence of 30% aqueous hydrogen peroxide afforded 1,2-bishydroperoxide 3, which could be cycloalkylated on treatment with silver oxide and a 1,ω-diiodoalkane to provide the tricyclic peroxides 12. Trimethyl

Synthesis, crystal structure and antimalarial activity of novel 1,2,5,6-tetraoxacycloalkanes from 2,3-dihydroperoxy-2-phenylnorbornane

McCullough, Kevin J.,Nonami, Yuji,Masuyama, Araki,Nojima, Masatomo,Kim, Hye-Sook,Wataya, Yusuke

, p. 9151 - 9155 (2007/10/03)

Photooxygenation of 2-phenylnorbornene 1 in the presence of 30% aqueous hydrogen peroxide in acetonitrile afforded the labile 1,2-bis-hydroperoxide 3 which could be cycloalkylated to provide the tricyclic peroxides 5, albeit in low yield, on treatment wit

Preparation and Reactivities of Hexakisacetonitrile Iron(III) Perchlorate and Related Complexes as Strong Oxidizing Reagents

Kotani,Eiichi,Kobayashi, Shigeki,Ishii, Yoko,Tobinaga, Seisho

, p. 4281 - 4291 (2007/10/02)

The iron(III) complexes Fe(S)6(ClO4)3, S=solvent, were prepared from Fe(H2O)6(ClO4)3 in the donor solvents.Reactions of alkylbenzenes with Fe(AN)6(ClO4)3 (AN=acetonitrile) were explored because the AN complex has the highest formal redox potential, E0=1.73 V vs.SCE, among these complexes.Oxidation of the primary alkylbenzenes by the iron(III) AN complex gave the corresponding acetamides (Table II).Oxidation of the secondary alkylbenzenes, namely, cumene, 2-phenylbutane, and 2-exo-phenylnorbornane, afforded the corresponding acetates and acetamides (Charts 2 and 3), consuming over 4-mol eq of reagent.Reactions of p-xylene and hexamethylbenzene with Fe(CH2=CHCN)6(ClO4)3 also yielded the amides 31a and 31b.These results demonstrate the applicability of the iron(III) AN complexes as a powerful reagent to oxidize organic substrates which have onset potentials of anodic current of ca. 2.0 V vs.SCE.Keywords - oxidation; primary alkylbenzene; secondary alkylbenzene; oxidizing reagent; iron(III) perchlorate solvate; hexakisacetonitrile iron(III) perchlorate; hexakisacrylonitrile iron(III) perchlorate

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