Interesting facts
Interesting Facts about 2-(Chloromethyl)oxirane
2-(Chloromethyl)oxirane, commonly known as a versatile epoxide, is a compound that showcases the fascinating complexity of organic chemistry. Here are some engaging highlights about this intriguing compound:
- Epoxide Structure: As an epoxide, 2-(chloromethyl)oxirane contains a three-membered cyclic ether, which is known for its unique reactivity and strain. This structure enables it to participate in various chemical reactions.
- Reactivity: The presence of the chloromethyl group enhances its reactivity, making it a valuable intermediate in organic synthesis. It can readily undergo ring-opening reactions, which can lead to a variety of functionalized compounds.
- Applications: This compound is utilized in multiple applications, including:
- As a key building block in the synthesis of pharmaceuticals and agrochemicals.
- In the production of polymer materials, enhancing their properties.
- Environmental Considerations: While 2-(chloromethyl)oxirane has excellent utility in synthesis, it is essential to handle such compounds with care due to potential toxicity and environmental impact. Researchers continually strive to understand and mitigate these effects.
- Historical Significance: The study of epoxides, including compounds like 2-(chloromethyl)oxirane, has significantly contributed to the field of synthetic organic chemistry. The exploration of their properties has led to breakthroughs in various domains, including biochemistry and material science.
In summary, 2-(chloromethyl)oxirane is not just a compound with a complex structure, but it also represents the dynamic nature of chemical research and development. Its applications and reactivity highlight the importance of understanding organic compounds in the advancement of technology and science.
Synonyms
EPICHLOROHYDRIN
2-(Chloromethyl)oxirane
106-89-8
Epichlorhydrin
1-Chloro-2,3-epoxypropane
Oxirane, (chloromethyl)-
Epichlorhydrine
Glycidyl chloride
Chloromethyloxirane
1,2-Epoxy-3-chloropropane
2,3-Epoxypropyl chloride
Chloropropylene oxide
Epichloorhydrine
3-Chloro-1,2-epoxypropane
Glycerol epichlorhydrin
Glycerol epichlorohydrin
3-Chloropropylene oxide
(Chloromethyl)ethylene oxide
Epicloridrina
(CHLOROMETHYL)OXIRANE
Epichlorohydryna
Epichlorophydrin
SKEKhG
epi-Chlorohydrin
alpha-Epichlorohydrin
3-Chloro-1,2-propylene oxide
2-Chloromethyl-oxirane
3-Chloropropene-1,2-oxide
(+/-)-Epichlorohydrin
Oxirane, 2-(chloromethyl)
epichlorohydrine
gamma-Chloropropylene oxide
1-Cloro-2,3-epossipropano
Propane, 1-chloro-2,3-epoxy-
1-Chlor-2,3-epoxy-propan
(RS)-3-chloro-1,2-epoxypropane
1-Chloor-2,3-epoxy-propaan
Epoxypropyl chloride
Rcra waste number U041
DL-a-Epichlorohydrin
Caswell No. 424
(+/-)-2-(Chloromethyl)oxirane
Allyl chloride oxide
NSC 6747
HSDB 39
Epoxy-3-chloropropane
CCRIS 277
(chloromethyl)-Oxirane
Chloropropylene
.alpha.-Epichlorohydrin
Oxirane,(chloromethyl)-
NCI-C07001
EINECS 203-439-8
Alyl chloride oxide
Chloropropyl epoxide
.gamma.-Chloropropylene oxide
EPA Pesticide Chemical Code 097201
UNII-08OOR508C0
(DL)-.alpha.-Epichlorohydrin
BRN 0079785
DTXSID1020566
CHEBI:37144
AI3-03545
08OOR508C0
NSC-6747
Chloro-1,2-epoxypropane
Chloro-2,3-epoxypropane
Chloropropene-1,2-oxide
3-Chloro-propylene oxide
2-(chloromethyl)-oxirane
MFCD00005132
(DL)-alpha-Epichlorohydrin
Chloro-1,2-propylene oxide
1-chloro-2,3-epoxy-propane
1-Chloro-2,3-epoxy propone
DTXCID50566
NSC6747
EC 203-439-8
(+/-)-1-Chloro-2,3-epoxypropane
13403-37-7
ECH
NCGC00091792-01
Epichlorohydrin, >=99%
EPICHLOROHYDRIN (IARC)
EPICHLOROHYDRIN [IARC]
EPICHLOROHYDRIN (MART.)
EPICHLOROHYDRIN [MART.]
Epicloridrina [Italian]
Epichloorhydrine [Dutch]
Epichlorhydrine [French]
Epichlorohydryna [Polish]
CAS-106-89-8
3-Chloropropyl epoxide
2-Chloropropylene oxide
dl-alpha-epichlorohydrin
5-17-01-00020 (Beilstein Handbook Reference)
UN2023
1-Chlor-2,3-epoxy-propan [German]
RCRA waste no. U041
1-Chloor-2,3-epoxy-propaan [Dutch]
1-Cloro-2,3-epossipropano [Italian]
epichiorohydrin
(chloromethyl) Ethylene oxide
Epichlorohydrin, (+-)-Isomer
epi-chlorohydrine
a-Epichlorohydrin
Epichloro hydrine
(rs)-epichlorohydrin
(+) epichlorohydrin
(-) epichlorohydrin
2-chloromethyloxirane
(?)-Epichlorohydrin
chloromethyl) Oxirane
(rac)-epichlorohydrin
racemic epichlorohydrin
(+-)-epichlorohydrin
a-Chloropropylene oxide
beta-epoxypropylchloride
racemic epichlorohydrine
Epichlorohydrin, 99%
Chloromethylethylene Oxide
2-(chloromethyl) Oxirane
ALPHA-EPICHOROHYDRIN
bmse000722
(RS)-EPICHLORHYDRIN
WLN: T3OTJ B1G
CRUDE EPICHLOROHYDRIN
(RS)-(chloromethyl)oxirane
EPICHLOROHYDRIN [MI]
oxirane, 2-(chloromethyl)-
EPICHLOROHYDRIN (DOT)
9009-12-5
3-Chloro-1,2-propane oxide
EPICHLOROHYDRIN [HSDB]
E181 [Russian epoxy resin]
NCI-CO7001
E 181 [Russian epoxy resin]
CHEMBL1421613
Tox21_111167
Tox21_200276
MSK001647
STL163564
AKOS000118974
AKOS016039400
Epichlorohydrin [UN2023] [Poison]
FE07765
SB11597
SB11598
UN 2023
3-CHLORO-1, 2-PROPYLENE OXIDE
NCGC00091792-02
NCGC00091792-03
NCGC00257830-01
BP-31004
BP-31046
(+/-)-Epichlorohydrin, analytical standard
DB-018066
DB-301965
Epichlorhydrin 1000 microg/mL in Methanol
J 006
NS00002426
( inverted exclamation markA)-Epichlorohydrin
EN300-19215
Epichlorhydrin 100 microg/mL in Cyclohexane.
Epichlorohydrin;3-Chloro-1,2-propylene oxide
(+/-)-Epichlorohydrin, purum, >=99% (GC)
CHLOROMETHYL (OXIRANE) (EPICHLOROHYDRIN)
Q423083
(+/-)-Epichlorohydrin, puriss., >=99.5% (GC)
F0001-0128
Z104473190
(+/-)-2-(Chloromethyl)oxirane, 1-Chloro-2,3-epoxypropane
(R)-(-)-1-Chloro-2,3-epoxypropane; 2-(Chloromethyl)oxirane
(S)-(+)-1-Chloro-2,3-epoxypropane; 2-(Chloromethyl)oxirane
203-439-8
Solubility of 2-(chloromethyl)oxirane
2-(chloromethyl)oxirane, also known as chloromethyl epoxy, possesses some intriguing properties regarding its solubility characteristics. This compound is a member of the epoxide family, which generally exhibits unique solubility behaviors due to their cyclic ether structure.
When considering the solubility of 2-(chloromethyl)oxirane, several key factors come into play:
As a rule of thumb, it can be stated that:
In summary, while 2-(chloromethyl)oxirane shows promising solubility in specific environments, it's essential to consider the nature of both the compound and the solvent. Understanding these solubility trends can be crucial for applications involving chemical reactions or formulations in which this compound is utilized. As you explore further, remember: “solubility is key to both safety and efficiency in chemical processes.”