CAS 2746-19-2
:(1α,2α,3β,6β)-1,2,3,6-tetrahydro-3,6-methanophthalic anhydride
Description:
(1α,2α,3β,6β)-1,2,3,6-tetrahydro-3,6-methanophthalic anhydride, with CAS number 2746-19-2, is a chemical compound characterized by its unique bicyclic structure, which includes a tetrahydro derivative of phthalic anhydride. This compound features a fused ring system that contributes to its stability and reactivity. It is typically a solid at room temperature and may exhibit a range of physical properties such as solubility in organic solvents. The presence of the anhydride functional group indicates that it can undergo hydrolysis to form corresponding acids, making it useful in various chemical reactions, including polymerization and as a building block in organic synthesis. Its stereochemistry, denoted by the specific alpha and beta configurations, plays a crucial role in determining its reactivity and interaction with other molecules. Overall, this compound is of interest in fields such as materials science and organic chemistry due to its potential applications in the development of new materials and chemical intermediates.
Formula:C9H8O3
InChI:InChI=1/C9H8O3/c10-8-6-4-1-2-5(3-4)7(6)9(11)12-8/h1-2,4-7H,3H2/t4?,5?,6-,7+
InChI key:InChIKey=KNDQHSIWLOJIGP-RNGGSSJXNA-N
SMILES:O=C1[C@]2([C@]([C@]3(C[C@@]2(C=C3)[H])[H])(C(=O)O1)[H])[H]
Synonyms:- (1alpha,2alpha,3beta,6beta)-1,2,3,6-Tetrahydro-3,6-methanophthalicanhydride
- (3aR,7aS)-3a,4,7,7a-tetrahydro-4,7-methano-2-benzofuran-1,3-dione
- 4,7-Methanoisobenzofuran-1,3-dione, 3a,4,7,7a-tetrahydro-, (3aR,4R,7S,7aS)-rel-
- 4,7-Methanoisobenzofuran-1,3-dione, 3a,4,7,7a-tetrahydro-, (3aalpha,4beta,7beta,7aalpha)-
- 4,7-Methanoisobenzofuran-1,3-dione, 3a,4,7,7a-tetrahydro-, (3aα,4β,7β,7aα)-
- 5-Norbornene-2,3-dicarboxylic anhydride, cis-exo-
- Bicyclo[2.2.1]Hept-5-Ene-Exo-2,3-Dicarboxylic Anhydride
- Bicyclo[2.2.1]hept-5-ene-2,3-di-exo-acid anhydride
- Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid exo-anhydride
- Exo-cis-5-Norbornene-2,3-dicarboxylic anhydride
- Himic anhydride
- Nsc 110659
- cis-5-Norbornene-exo-2,3-dicarboxylic anhydride
- cis-5-Norbornene-exo-anhydride
- cis-Norbornene-exo-2,3-dicarboxylic anhydride
- exo,exo-2,3-Norborn-5-enedicarboxylic anhydride
- exo-2,3-Norbornenedicarboxylic acid anhydride
- exo-3,6-Methylene-1,2,3,6-tetrahydrophthalic anhydride
- exo-3,6-Methylene-4-cyclohexene-1,2-dicarboxylic anhydride
- exo-5-Norbornene-1,2-dicarboxylic anhydride
- exo-5-Norbornene-2,3-dicarboxylic anhydride
- exo-Carbic anhydride
- exo-Nadic anhydride
- exo-Norbornene dicarboxylic anhydride
- exo-cis-3,6-endo-Methylene-Δ<sup>4</sup>-tetrahydrophthalic anhydride
- rel-(3aR,4R,7S,7aS)-3a,4,7,7a-Tetrahydro-4,7-methanoisobenzofuran-1,3-dione
- exo-cis-3,6-endo-Methylene-Δ4-tetrahydrophthalic anhydride
- (1α,2β,6β,7α)-4-Oxatricyclo[5.2.1.02,6]deca-8-ene-3,5-dione
- (1S,2R,6S,7S)-4-oxatricyclo[5.2.1.0^{2,6}]dec-8-ene-3,5-dione
- Norborn-5-ene-2,3-dicarboxylicanhydride2-exo,3-exoisomere
- (2-exo,3-exo)-Norborn-5-ene-2,3-dicarboxylic acid anhydride, exo-cis-Himic anhydride
- (3aS)-3aα,4,7,7aα-Tetrahydro-4β,7β-methanoisobenzofuran-1,3-dione
- (3at,7at)-3a,4,7,7a-tetrahydro-4r,7c-methano-isobenzofuran-1,3-dione
- (1α,2α,3β,6{f1b})-1,2,3,6-tetrahydro-3,6-methanophthalicanhydride
- CIS-5-NORBORNENE-EXO-2,3-DICARBOXYLIC AN
- (3aR,7aS)-3a,4,7,7a-tetrahydro-4,7-Methanoisobenzofuran-1,3-dione
- norborn-5-ene-2exo,3exo-dicarboxylicacidanhydride
- (3aR,4R,7S,7aS)-rel-3a,4,7,7a-Tetrahydro-4,7-Methanoisobenzofuran-1,3-dione
- cis
- (1α,2α,3β,6β)-1,2,3,6-tetrahydro-3,6-Methanophthalic anhydride
- (1β,2α,6α,7β)-4-Oxatricyclo[5.2.1.02,6]decane-8-ene-3,5-dione
- (3aR,4R,7S,7aS)-3a,4,7,7a-tetrahydro-4,7-Methanoisobenzofurn-1,3-dione
- (2-exo,3-exo)-Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid anhydride
- (1R,1β,4S)-Norborna-5-ene-2β,3β-dicarboxylic anhydride
- 3at,7at-3a,4,7,7a-tetrahydro-4r,7c-methano-isobenzofuran-1,3-dione
- 4,7-Methanoisobenzofuran-1,3-dione,3a,4,7,7a-tetrahydro-, (3
- cis-5-Norbornene-exo-2,3-dicarboxylic anhydride,95%
- (1alpha,2alpha,3beta,6beta)-1,2,3,6-tetrahydro-3,6-methanophthalic anhydride
- bicyclo(2.2.1)heptene-5-exo-2,3-dicarboxylicanhydride
- (3aR)-3aβ,4,7,7aβ-Tetrahydro-4α,7α-methanoisobenzofuran-1,3-dione
- (1R,2α,6α,7S)-4-Oxatricyclo[5.2.1.02,6]deca-8-ene-3,5-dione
- -5-Norbornene-exo-2,3-dicarboxylic anhydride
- See more synonyms
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Found 10 products.
cis-5-Norbornene-exo-2,3-dicarboxylic Anhydride
CAS:Formula:C9H8O3Purity:>97.0%(GC)(T)Color and Shape:White to Almost white powder to crystalMolecular weight:164.16cis-5-Norbornene-exo-2,3-dicarboxylic anhydride, 95%
CAS:<p>cis-5-Norbornene-exo-2,3-dicarboxylic anhydride is used as an organic chemical synthesis intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aes</p>Formula:C9H8O3Purity:95%Molecular weight:164.164,7-Methanoisobenzofuran-1,3-dione, 3a,4,7,7a-tetrahydro-,(3aR,4R,7S,7aS)-rel-
CAS:Formula:C9H8O3Purity:97%Color and Shape:SolidMolecular weight:164.1580Cis-5-Norbornene-exo-2,3-dicarboxylic Anhydride
CAS:Cis-5-Norbornene-exo-2,3-dicarboxylic AnhydridePurity:≥98%Molecular weight:164.16g/mol(2-exo,3-exo)-Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid anhydride
CAS:<p>(2-exo,3-exo)-Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid anhydride</p>Formula:C9H8O3Purity:97%Color and Shape: white solidMolecular weight:164.16g/molCis-5-Norbornene-exo-2,3-dicarboxylic Anhydride
CAS:<p>Cis-5-Norbornene-exo-2,3-dicarboxylic Anhydride: sensitizing, induces HepG2/SK-Hep1 apoptosis, inhibits PP2A. IC50: HepG2=62μM, SK-Hep1=151μM.</p>Formula:C9H8O3Purity:99.32%Color and Shape:SolidMolecular weight:164.16cis-Norbornene-exo-2,3-dicarboxylic anhydride
CAS:<p>Cis-Norbornene-exo-2,3-dicarboxylic anhydride is a reactive compound that is used as a precursor in the production of other chemicals. It can be used as an oxidation catalyst for organic synthesis reactions and has been shown to have high reactivity with hydroxyl groups under acidic conditions. Cis-Norbornene-exo-2,3-dicarboxylic anhydride reacts with calcium stearate to form a variety of products including aromatic hydrocarbons and boron nitride. The solubility data for cis-Norbornene-exo-2,3-dicarboxylic anhydride in human serum is available. The quantum theory predicts that cis-Norbornene-exo-2,3-dicarboxylic anhydride will undergo cationic polymerization in an acidic environment. This product also reacts with fatty acids to produce al</p>Formula:C9H8O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:164.16 g/molcis-5-Norbornene-exo-2,3-dicarboxylic Anhydride
CAS:Formula:C9H8O3Purity:95%Color and Shape:Solid, Crystalline Powder or PowderMolecular weight:164.16cis-Norbornene-exo-2,3-dicarboxylic Anhydride
CAS:Controlled Product<p>Applications cis-Norbornene-exo-2,3-dicarboxylic Anhydride (cas# 2746-19-2) is a compound useful in organic synthesis.<br></p>Formula:C9H8O3Color and Shape:NeatMolecular weight:164.16
![(2-exo,3-exo)-Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid anhydride](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F54%2Fthumb%2FOR46134.jpg&w=3840&q=75)
