Interesting facts
Interesting Facts about Methyl Carbonochloridate
Methyl carbonochloridate, commonly referred to as a reagent in organic synthesis, is an intriguing compound with a variety of applications in chemistry. Here are some noteworthy aspects of this compound:
- Reactivity: Methyl carbonochloridate is an excellent electrophile, making it highly reactive towards nucleophiles. This property is particularly valued in the formation of esters and acyl chlorides.
- Synthesis: It is often synthesized from the reaction of methyl chloroformate with various reagents. The ability to create this compound opens doors for the preparation of more complex molecular structures.
- Versatile Use: Methyl carbonochloridate is used in the synthesis of various pharmaceuticals and agrochemicals, significantly contributing to the development of effective drugs and crop protection agents.
- Toxicity: While useful, this compound is also toxic; hence, proper safety precautions and handling procedures are essential when working with it in the laboratory.
- Chlorination Importance: The presence of chlorine in this compound plays a vital role in its reactivity and stability, making it popular in chlorination reactions within organic chemistry.
In conclusion, Methyl carbonochloridate serves as an essential tool for chemists, exemplifying the balance between utility and caution in chemical handling. As one researcher aptly noted, "A careful approach to its reactivity can yield innovative solutions in organic synthesis."
Synonyms
METHYL CHLOROFORMATE
79-22-1
Methyl chlorocarbonate
methyl carbonochloridate
Chloroformic acid methyl ester
Methoxycarbonyl chloride
Metilcloroformiato
K-Stoff
Methylchloorformiaat
Carbonochloridic acid, methyl ester
RCRA waste number U156
Methyl chloridocarbonate
Formic acid, chloro-, methyl ester
Chloroformiate de methyle
Chlorocarbonic acid methyl ester
Chlorocarbonate de methyle
Methylchloorformiaat [Dutch]
Metilcloroformiato [Italian]
Chlorameisensaeure methylester
TL 438
HSDB 1116
Methylester kyseliny chlormravenci
Methylester kyseliny chloruhlicite
RC6VA8OB2N
Chloroformiate de methyle [French]
Chlorocarbonate de methyle [French]
EINECS 201-187-3
UN1238
Chlorameisensaeure methylester [German]
BRN 0605437
DTXSID0024185
Methylester kyseliny chlormravenci [Czech]
Methylester kyseliny chloruhlicite [Czech]
Carbonochloridic acid methyl ester
MFCD00000639
DTXCID004185
Chlorocarbonic acid, methyl ester
EC 201-187-3
METHYL CHLOROCARBONATE [MI]
METHYL CHLOROFORMATE [HSDB]
METHYLCHLOORFORMIAAT (DUTCH)
METILCLOROFORMIATO (ITALIAN)
CHLOROFORMIATE DE METHYLE (FRENCH)
CHLOROCARBONATE DE METHYLE (FRENCH)
CHLORAMEISENSAEURE METHYLESTER (GERMAN)
chloro(methoxy)methanone
METHYLCHLOROFORMATE
UNII-RC6VA8OB2N
RCRA waste no. U156
KStoff
methylchoroformate
Carbonochloridic acid, methylester
methy chloroformate
methyl chloroformat
methyl choroformate
ClCOOMe
MeOCOCl
methyl chioroformate
methyl-chloroformate
Chlorocarbonic Acid Methyl Ester; Methoxycarbonyl Chloride; Methyl Carbonochloridate; Methyl Chlorocarbonate; Methyl Chloroformate
methylchlorocarbonate
methyl chloroforrnate
ClCO2Me
methyl chloroform ate
methoxycarbonylchloride
methylcarbonochloridate
methylchloridocarbonate
CH3OCOCl
methyl carbonchloridate
MeOC(O)Cl
ClCO2CH3
chloro-(methoxy)methanone
Methyl chloridocarbonate #
Methyl chloroformate, 99%
chloro formic acid methyl ester
CHEMBL3182300
XMJHPCRAQCTCFT-UHFFFAOYSA-
Formic acid, chloro, methyl ester
Tox21_200841
BBL011482
STL146594
AKOS000121088
CHLOROFORMIC ACID, METHYL ESTER
UN 1238
CAS-79-22-1
NCGC00248847-01
NCGC00258395-01
BP-31038
Methyl chloroformate [UN1238] [Poison]
NS00002965
InChI=1/C2H3ClO2/c1-5-2(3)4/h1H3
Q419678
201-187-3
Solubility of Methyl Carbonochloridate
Methyl carbonochloridate, with the chemical formula C3H4ClO2, exhibits interesting solubility characteristics that are worth noting:
In summary, while methyl carbonochloridate's solubility in water may be limited, it shows promising solubility in various organic solvents, making it versatile for different chemical applications. Understanding its solubility behavior is crucial for effectively utilizing this compound in laboratory practices.