Cas no 1392212-84-8 (2-(chloromethyl)oxirane, prop-2-en-1-amine)

2-(Chloromethyl)oxirane, also known as epichlorohydrin, is a highly reactive epoxide compound widely used as an intermediate in the synthesis of epoxy resins, glycidyl ethers, and other specialty chemicals. Its bifunctional nature (epoxide and chloromethyl groups) enables versatile crosslinking and polymerization reactions, making it valuable in adhesives, coatings, and elastomers. Prop-2-en-1-amine (allylamine) is an unsaturated amine with a reactive double bond and primary amine group, serving as a key building block in pharmaceuticals, agrochemicals, and polymer modification. Its dual functionality allows for nucleophilic addition and radical polymerization, facilitating the production of functionalized polymers and bioactive compounds. Both compounds offer high reactivity and selectivity, essential for advanced chemical synthesis.
2-(chloromethyl)oxirane, prop-2-en-1-amine structure
1392212-84-8 structure
Product Name:2-(chloromethyl)oxirane, prop-2-en-1-amine
CAS No:1392212-84-8
MF:C6H12ClNO
MW:149.618580818176
CID:6060184
PubChem ID:3085017
Update Time:2025-10-28

2-(chloromethyl)oxirane, prop-2-en-1-amine Chemical and Physical Properties

Names and Identifiers

    • 2-(chloromethyl)oxirane, prop-2-en-1-amine
    • 2-(chloromethyl)oxirane:prop-2-en-1-amine
    • ZNSIZMQNQCNRBW-UHFFFAOYSA-N
    • EN300-25310384
    • CHEMBL1201798
    • 52757-95-6
    • 2-(chloromethyl)oxirane; prop-2-en-1-amine
    • Sevelamer anhydrous
    • 1392212-84-8
    • DB00658
    • D08512
    • Sevelamer Hydrochloride (Technical Grade)
    • NCGC00522026-01
    • Sevelamer
    • 2-(chloromethyl)oxirane;prop-2-en-1-amine
    • 2-Propen-1-amine, polymer with (chloromethyl)oxiraneOTHER CA INDEX NAMES:Oxirane, (chloromethyl)-, polymer with 2-propen-1-amine
    • 3-(Trifluoromethoxy)cinnamicacid
    • SCHEMBL726092
    • Sevelamer (INN)
    • Inchi: 1S/C3H5ClO.C3H7N/c4-1-3-2-5-3;1-2-3-4/h3H,1-2H2;2H,1,3-4H2
    • InChI Key: ZNSIZMQNQCNRBW-UHFFFAOYSA-N
    • SMILES: C(C1OC1)Cl.C(=C)CN

Computed Properties

  • Exact Mass: 149.0607417g/mol
  • Monoisotopic Mass: 149.0607417g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 2
  • Complexity: 55.1
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 38.6?2

2-(chloromethyl)oxirane, prop-2-en-1-amine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Enamine
EN300-25310384-0.05g
2-(chloromethyl)oxirane, prop-2-en-1-amine
1392212-84-8 95%
0.05g
$148.0 2024-06-19

Additional information on 2-(chloromethyl)oxirane, prop-2-en-1-amine

Comprehensive Overview of 2-(chloromethyl)oxirane and prop-2-en-1-amine (CAS No. 1392212-84-8)

2-(chloromethyl)oxirane, also known as epichlorohydrin, and prop-2-en-1-amine, commonly referred to as allylamine, are versatile chemical compounds with significant applications in industrial and research settings. These compounds are widely studied due to their unique reactivity and utility in synthesizing polymers, pharmaceuticals, and specialty chemicals. Their CAS No. 1392212-84-8 designation ensures precise identification in regulatory and scientific databases, making them critical for compliance and innovation.

The growing interest in sustainable chemistry and green synthesis has placed compounds like 2-(chloromethyl)oxirane and prop-2-en-1-amine at the forefront of research. Researchers and manufacturers are increasingly exploring eco-friendly derivatization methods to reduce environmental impact. For instance, bio-based epoxides and amine-functionalized polymers are trending topics, aligning with global demands for circular economy practices. These trends highlight the relevance of these compounds in modern chemical innovation.

From a structural perspective, 2-(chloromethyl)oxirane features an epoxide ring and a chloromethyl group, enabling nucleophilic ring-opening reactions. This reactivity is exploited in producing epoxy resins, adhesives, and coatings. Meanwhile, prop-2-en-1-amine’s allylic amine structure is pivotal in creating pharmaceutical intermediates and agrochemicals. Users frequently search for "epichlorohydrin substitutes" or "allylamine derivatives," reflecting the need for safer alternatives and novel applications.

In the pharmaceutical sector, prop-2-en-1-amine is a key building block for antifungal agents and anticancer drugs. Its incorporation into small-molecule therapeutics underscores its importance in drug discovery. Similarly, 2-(chloromethyl)oxirane is integral to cross-linking agents used in controlled-release formulations. Searches like "amine-functionalized drug delivery" or "epoxide stability in APIs" demonstrate the intersection of these compounds with cutting-edge medical research.

Industrial applications of CAS No. 1392212-84-8 span textile auxiliaries, water treatment chemicals, and composite materials. The demand for high-performance polymers has surged, driven by sectors like automotive and aerospace. Queries such as "epoxy resin mechanical properties" or "allylamine copolymer uses" indicate user interest in material science advancements. These compounds’ adaptability to nanotechnology and smart materials further enhances their market appeal.

Safety and handling of 2-(chloromethyl)oxirane and prop-2-en-1-amine are critical discussion points. While not classified as hazardous under standard conditions, proper storage protocols and personal protective equipment (PPE) are emphasized in technical guidelines. Users often seek "safe handling of epoxides" or "amine stability in storage," reflecting a focus on operational safety. Regulatory frameworks like REACH and GHS provide guidelines for their compliant use.

Innovation continues to drive the applications of these compounds. Recent studies explore their roles in renewable energy systems, such as fuel cell membranes and battery electrolytes. The rise of bio-based amines and epoxide-modified biomaterials aligns with the push for carbon-neutral solutions. Searches for "green epoxy alternatives" or "allylamine in energy storage" highlight these emerging trends.

In summary, 2-(chloromethyl)oxirane and prop-2-en-1-amine (CAS No. 1392212-84-8) are indispensable in modern chemistry. Their versatility in polymer science, pharmaceuticals, and sustainable technologies ensures ongoing relevance. By addressing user queries and industry trends, this overview bridges scientific depth with practical insights, fostering informed decision-making for researchers and manufacturers alike.

Recommended suppliers
Shandong Jing Kun Chemical Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Jing Kun Chemical Co.,Ltd.
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Hubei Cuiyuan Biotechnology Co.,Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hubei Cuiyuan Biotechnology Co.,Ltd
Hunan Well Medicine Synthesis Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hunan Well Medicine Synthesis Technology Co., Ltd.
Shenzhen Yaoyuan R&D Center Co.,Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shenzhen Yaoyuan R&D Center Co.,Ltd