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· · COA & SDS available for every product · Same-day shipping on in-stock items 1,4-dimethyl bicyclo[2.2.1]heptane-1,4-dicarboxylate - ≥97% , CAS No.15448-76-7
Synonyms
A883720 | UBGSPDWVUMFEAZ-UHFFFAOYSA-N | SY103455 | bicyclo[2.2.1]heptane-1,4-dicarboxylate | Bicyclo[2.2.1]heptane-1,4-dicarboxylic acid, dimethyl ester | AMY34081 | EN300-174111 | SB12249 | AKOS016007414 | Dimethyl bicyclo[2.2.1]heptane-1,4-carboxylate |
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
A883720 | UBGSPDWVUMFEAZ-UHFFFAOYSA-N | SY103455 | bicyclo[2.2.1]heptane-1, 4-dicarboxylate | Bicyclo[2.2.1]heptane-1, 4-dicarboxylic acid, dimethyl ester | AMY34081 | EN300-174111 | SB12249 | AKOS016007414 | Dimethyl bicyclo[2.2.1]heptane-1, 4-carboxylate |
Specifications & Purity
≥97%
Names and Identifiers Canonical Smiles COC(=O)C12CCC(C1)(CC2)C(=O)OC IUPAC Name dimethyl bicyclo[2.2.1]heptane-1,4-dicarboxylate InChIKey UBGSPDWVUMFEAZ-UHFFFAOYSA-N INCHI 1S/C11H16O4/c1-14-8(12)10-3-5-11(7-10,6-4-10)9(13)15-2/h3-7H2,1-2H3 Isomeric SMILES COC(=O)C12CCC(C1)(CC2)C(=O)OC Molecular Weight 212.24 Reaxy-Rn 3094903 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3094903&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Lipids and lipid-like molecules Class Prenol lipids Subclass Monoterpenoids Intermediate Tree Nodes Not available Direct Parent Bicyclic monoterpenoids Alternative Parents Dicarboxylic acids and derivatives Methyl esters Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic homopolycyclic compounds Substituents Bicyclic monoterpenoid - Dicarboxylic acid or derivatives - Methyl ester - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 212.240 g/mol XLogP3 0.900 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 4 Exact Mass 212.105 Da Monoisotopic Mass 212.105 Da Topological Polar Surface Area 52.600 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 270.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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