Isobornyl Acrylate (stabilized with MEHQ) (copy) - ≥90%(GC) , CAS No.5888-33-5

CAS: 5888-33-5 Cat. No.: I418711 Molecular Weight: 208.3 EC Number: 227-561-6

GRADE & PURITY ≥90%(GC)

Synonyms

QM 589 | exo-1,7,7-Trimethylbicyclo(2.2.1)hept-2-yl acrylate | MFCD00080424 | DS-7769 | Light Acrylate IB-XA | EC 227-561-6 | 2-Propenoic acid, 1,7,7-trimethylbicyclo(2.2.1)hept-2-yl ester, exo- | SR 506 (acrylate) | EINECS 227-561-6 | ISOBORNYL ACRYLATE

Storage

Protected from light,Room temperature,Cool

Shipped In

Normal

Overview

Isobornyl acrylate (IBA) can be used to prepare block copolymers with n-butyl acrylate by atom transfer radical polymerization (ATRP).

Specifications

Synonyms

QM 589 | exo-1, 7, 7-Trimethylbicyclo(2.2.1)hept-2-yl acrylate | MFCD00080424 | DS-7769 | Light Acrylate IB-XA | EC 227-561-6 | 2-Propenoic acid, 1, 7, 7-trimethylbicyclo(2.2.1)hept-2-yl ester, exo- | SR 506 (acrylate) | EINECS 227-561-6 | ISOBORNYL ACRYLATE

Specifications & Purity

≥90%(GC)

Storage

Protected from light, Room temperature, Cool

Shipped In

Normal

Purity

≥90%(GC)

Names and Identifiers

• Pubchem Sid: 504759674
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504759674
• Canonical Smiles: CC1(C2CCC1(C(C2)OC(=O)C=C)C)C
• IUPAC Name: [(1R,2R,4R)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] prop-2-enoate
• InChIKey: PSGCQDPCAWOCSH-BREBYQMCSA-N
• INCHI: 1S/C13H20O2/c1-5-11(14)15-10-8-9-6-7-13(10,4)12(9,2)3/h5,9-10H,1,6-8H2,2-4H3/t9-,10-,13+/m1/s1
• Isomeric SMILES: C[C@@]12CC[C@@H](C1(C)C)C[C@H]2OC(=O)C=C
• WGK Germany: 2
• RTECS: UD3940000
• UN Number: 3082
• Packing Group: II
• Molecular Weight: 208.3
• Reaxy-Rn: 2254825
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2254825&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Prenol lipids
      • Subclass Monoterpenoids

• 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: Acrylic acid esters Enoate esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Bicyclic monoterpenoid - Bornane monoterpenoid - Acrylic acid ester - Acrylic acid or derivatives - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - 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.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Difficult to mix in water.
• Sensitivity: light sensitive
• Refractive Index: 1.48
• Flash Point(°F): 206.6 °F
• Flash Point(°C): 97 °C
• Boil Point(°C): 119-121°C/15mmHg
• Molecular Weight: 208.300 g/mol
• XLogP3: 3.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 208.146 Da
• Monoisotopic Mass: 208.146 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 306.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• 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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