Fenchyl Alcohol - ≥96%(GC) , CAS No.1632-73-1

CAS: 1632-73-1 Cat. No.: F156588 Peso molecular: 154.25 Número EC: 216-639-5

GRADE & PURITY ≥96%(GC)

Synonyms

CAS-1632-73-1 | CCG-266251 | Q417941 | SCHEMBL58038 | AKOS006230299 | s5379 | Bicyclo(2.2.1)heptan-2-ol, 1,3,3-trimethyl- | (1S,2S,4R)-1,3,3-Trimethyl-bicyclo[2.2.1]heptan-2-ol | 410Q2GK1HF | 1,3,3-TRIMETHYL-2-NORBORNANOL | EN300-296384 | SY115529 | FENCH

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

CAS-1632-73-1 | CCG-266251 | Q417941 | SCHEMBL58038 | AKOS006230299 | s5379 | Bicyclo(2.2.1)heptan-2-ol, 1, 3, 3-trimethyl- | (1S, 2S, 4R)-1, 3, 3-Trimethyl-bicyclo[2.2.1]heptan-2-ol | 410Q2GK1HF | 1, 3, 3-TRIMETHYL-2-NORBORNANOL | EN300-296384 | SY115529 | FENCH

Especificaciones y pureza

≥96%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥96%(GC)

Nombres e identificadores

• Pubchem Sid: 504752659
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752659
• Sonrisas canónicas: CC1(C2CCC(C2)(C1O)C)C
• IUPAC Name: 1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
• InChIKey: IAIHUHQCLTYTSF-UHFFFAOYSA-N
• INCHI: 1S/C10H18O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7-8,11H,4-6H2,1-3H3
• Isómeros SMILES: CC1(C2CCC(C2)(C1O)C)C
• RTECS: DT5080000
• Peso molecular: 154.25
• Reaxy-Rn: 1850917
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1850917&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Bicyclic monoterpenoids
• Alternative Parents: Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Fenchane monoterpenoid - Bicyclic monoterpenoid - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound
• Descripción: 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: a monoterpenol

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

Objetivos asociados (humanos)

UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)

Discover Target: UGT1A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DGAT1 Tclin Diacylglycerol O-acyltransferase 1 (1719 Activities)

Discover Target: DGAT1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UGT2A1 UDP-glucuronosyltransferase 2A1 (59 Activities)

Discover Target: UGT2A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Leptinotarsa decemlineata (1161 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in Methanol
• Índice de refracción: 1.48
• Punto de inflamación (°F): 74°C(lit.)
• Punto de inflamación (°C): 74°C(lit.)
• Punto de ebullición (°C): 202 °C
• Punto de fusión (°C): 47°C(lit.)
• Peso molecular: 154.250 g/mol
• XLogP3: 2.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 154.136 Da
• Monoisotopic Mass: 154.136 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 185.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 3
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Xiaojiao Zheng, Weiwei Ma, Qihui Wang, Yaping Xu, Yukun Yang, Shu Qin, Xu Jing.  (2023)  Development of self-dispersion ferrofluid-based dispersive liquid–liquid microextraction for determining chiral fungicide hexaconazole in water, tea, and juice using high-performance liquid chromatography.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2023.109593]

2. Yunchang Fan, Hui Luo, Chunyan Zhu, Wenjin Li, Di Wu, Hongwei Wu.  (2021)  Hydrophobic natural alcohols based deep eutectic solvents: Effective solvents for the extraction of quinine.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2021.119112]

3. Cuicui Zhou, Yuxin Xiang, Chaoxi Zeng, Feiyang Li, Yuanjie Wu, Haoren Wu, Yong Yuan, Jin Cao, Feiyan Yin, Jianhui Ye, Zhonghua Liu, Meng Shi.  (2025)  Mechanistic insights into the stabilization of sulforaphane mediated by natural alcohol-derived hydrophobic deep eutectic solvents.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2025.118910]

4. Hu Wenxu, Ge Dandan, Fu Feie, Yuan Lin, Yang Chunyan, Weng Zhehui, Huang Yao.  (2026)  Supramolecular solvents based on deep eutectic solvents and hexafluorobutanol for the extraction of aristolochic acids from natural plants.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,      [PMID:41642342] [10.1007/s00216-026-06357-w]