2-(2-Chloroethoxy)ethanol - ≥98% , CAS No.628-89-7

CAS: 628-89-7 Cat. No.: C118686 Fórmula: ClCH₂CH₂OCH₂CH₂OH Peso molecular: 124.57 Beilstein Registry Number: 506015 Número CE: 211-059-9

GRADE & PURITY ≥98%

Synonyms

2-(2-chloro ethoxy)ethanol | EC 211-059-9 | UNII-R2UP818L4I | GS-3037 | R2UP818L4I | WLN: QZO2G | Q27287714 | LECMBPWEOVZHKN-UHFFFAOYSA- | 2-(2-chloroethoxy) ethanol | 2(2-chloroethoxy) ethanol | 2-(2-chloroethoxyl)ethanol | 2-(2-chloroethoxyl)-ethanol |

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Visão geral

2-(2-Chloroethoxy)ethanol was used in the synthesis of o-nitrophenylbromoacetaldehyde bis-2-(2-chloroethoxy)-ethyl acetal, quetiapine (an antipsychotic drug) and 2-(2-azidoethoxy)ethanol.

Specifications

Sinónimos

2-(2-chloro ethoxy)ethanol | EC 211-059-9 | UNII-R2UP818L4I | GS-3037 | R2UP818L4I | WLN: QZO2G | Q27287714 | LECMBPWEOVZHKN-UHFFFAOYSA- | 2-(2-chloroethoxy) ethanol | 2(2-chloroethoxy) ethanol | 2-(2-chloroethoxyl)ethanol | 2-(2-chloroethoxyl)-ethanol |

Especificações e pureza

≥98%

Condições de armazenamento de armazenamento

Store at 2-8°C,Argon charged

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Pureza

≥98%

Nomes e identificadores

• Pubchem Sid: 508807854
• Sorrisos canónicos: C(COCCCl)O
• IUPAC Name: 2-(2-chloroethoxy)ethanol
• InChIKey: LECMBPWEOVZHKN-UHFFFAOYSA-N
• INCHI: 1S/C4H9ClO2/c5-1-3-7-4-2-6/h6H,1-4H2
• SMILES isoméricas: C(COCCCl)O
• WGK Alemanha: 2
• RTECS: KK1350000
• Peso molecular: 124.57
• Beilstein: 506015
• Reaxy-Rn: 506015
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506015&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Primary alcohols Organochlorides Hydrocarbon derivatives Alkyl chlorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyl ether - Hydrocarbon derivative - Primary alcohol - Organochloride - Organohalogen compound - Alkyl halide - Alkyl chloride - Alcohol - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
• 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

Propriedades químicas e físicas

• Solubilidade: Miscible with water.
• Sensibilidade: Moisture and Heat sensitive
• Índice de refração: 1.452
• Ponto de inflamação (°F): 194 °F
• Ponto de inflamação (°C): 90°C
• Ponto de ebulição (°C): 79-81°C
• Peso molecular: 124.560 g/mol
• XLogP3: 0.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 124.029 Da
• Monoisotopic Mass: 124.029 Da
• Topological Polar Surface Area: 29.500 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 32.900
• 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

Referências

1. Yunchang Fan, Dongxu Cai, Lei Yang, Xiaoyuan Chen, Lei Zhang.  (2019)  Extraction behavior of nicotinic acid and nicotinamide in ionic liquids.  CHEMICAL ENGINEERING RESEARCH & DESIGN,      [PMID:] [10.1016/j.cherd.2019.04.017]

2. Song Zou, Guichun He, Xinyang Yu, Hong Zhong.  (2024)  Three novel dithiocarbamate surfactants: Synthesis, DFT calculation and flotation mechanism to chalcopyrite.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2024.125993]

3. Rihui Liang, Maoxin Zhang, Bo Yuan, Wei Feng.  (2025)  Regulation of Molecular Solar Thermal Energy Storage Capacity of Azobenzene and Acrylic Ester Copolymers through Hydrogen Bonding and Application in Solar Thermal Cells.  ACS Applied Materials & Interfaces,      [PMID:40662601] [10.1021/acsami.5c05615]

4. Yuanyuan Zhou, Qingyang Xiao, Shaohua Yang, Shuchun Yu.  (2026)  Design of high-performance branched Poly(aryl ether isatin) anion exchange membrane based on hydrogen bonding regulation.  JOURNAL OF POWER SOURCES,      [PMID:] [10.1016/j.jpowsour.2026.239393]