cis-3-Hexenyl crotonate - ≥95% , CAS No.65405-80-3

CAS: 65405-80-3 Cat. No.: C154063 Formula: C₁₀H₁₆O₂ Molecular Weight: 168.24 EC Number: 265-746-3

GRADE & PURITY ≥95%

Synonyms

BCP9000290 | FT-0681734 | SCHEMBL15536312 | Crotonic Acid cis-3-Hexen-1-yl Ester | (3Z)-3-hexen-1-yl ester(2E)-2-Butenoic acid | 2-IMINOPIPERIDINEHYDROCHLORIDE | 4SW5S1T63S | (3z)-3-hexenyl Ester(2e)-2-butenoic Acid | cis-3-Hexen-1-yl Crotonate | DTXSID90

Storage

Protected from light,Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

BCP9000290 | FT-0681734 | SCHEMBL15536312 | Crotonic Acid cis-3-Hexen-1-yl Ester | (3Z)-3-hexen-1-yl ester(2E)-2-Butenoic acid | 2-IMINOPIPERIDINEHYDROCHLORIDE | 4SW5S1T63S | (3z)-3-hexenyl Ester(2e)-2-butenoic Acid | cis-3-Hexen-1-yl Crotonate | DTXSID90

Specifications & Purity

≥95%

Storage

Protected from light,Argon charged,Room temperature

Shipped In

Normal

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 508811365
• Canonical Smiles: CCC=CCCOC(=O)C=CC
• IUPAC Name: [(Z)-hex-3-enyl] (E)-but-2-enoate
• InChIKey: KITGYVIOYOCIIE-QNMAEOQASA-N
• INCHI: 1S/C10H16O2/c1-3-5-6-7-9-12-10(11)8-4-2/h4-6,8H,3,7,9H2,1-2H3/b6-5-,8-4+
• Isomeric SMILES: CC/C=C\CCOC(=O)/C=C/C
• Molecular Weight: 168.24
• Reaxy-Rn: 27031287
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=27031287&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Fatty Acyls
      • Subclass Fatty acid esters

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Fatty Acyls
• Subclass: Fatty acid esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty acid esters
• Alternative Parents: Enoate esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty acid ester - 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 acyclic compound
• Description: This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.
• 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

• Sensitivity: Light sensitive
• x_refractive_index: 1.455
• x_flash_point_drop_fahrenheit: 94°C(lit.)
• x_flash_point_drop_centigrade: 94°C(lit.)
• x_boil_point_char: 107℃
• Molecular Weight: 168.230 g/mol
• XLogP3: 2.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 168.115 Da
• Monoisotopic Mass: 168.115 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 169.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 2
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 2
• Covalently-Bonded Unit Count: 1