79-22-1 Usage
Chemical Properties
Methyl chloroformate is a colorless liquid with an unpleasant, acrid odor. This is a highly corrosive and flammable material. Decomposed by hot water; stable to cold water. Soluble in methanol alcohol, ether, and benzene.
Uses
Chloroformic Acid Methyl Ester is used in the synthesis of a new class of potent Cdk4 inhibitors in the treatment of cancer. Also used in the synthesis of Phorboxazole B.
Production Methods
Prepared from phosgene and methyl alcohol.
Application
Methyl chloroformate (MCF) is generally used for the derivatization of functional groups such as carboxylic acids, amines, and phenols.MCF can also be used:To activate 3-acylpyridines for nucleophilic addition with alkynyltin reagents to form 2,3-disubstituted 1,2-dihydropyridines.Chloroesterification of terminal alkynes to form β-chloro-α,β-unsaturated esters.As an electrophilic reagent to mediate the reaction of pyridine with lithium dialkyl- or diarylcuprates to form 4-substituted 1,4-dihydropyridine derivatives.To convert nitronates into methoxycarbonyl nitronates.
General Description
A colorless liquid with a pungent odor. Flash point 54°F. Corrosive to metals and tissue. Vapors heavier than air. Very toxic by inhalation. Used to make other chemicals and insecticides.
Air & Water Reactions
Highly flammable. Gives off hydrochloric acid fumes in contact with moist air. Slightly soluble in water and decomposed by water to hydrochloric acid with evolution of heat.
Reactivity Profile
Methyl chloroformate is incompatible with water, strong oxidizing agents, alcohols, bases (including amines). Decomposes slowly in water to yield methanol, HCl, and CO2; reaction can be hazardous if water is hot. Attacks many metals especially in humid atmosphere [Handling Chemicals Safely 1980. p. 476]. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291].
Hazard
Flammable, dangerous fire risk. Highly corrosive and irritant to skin and eyes.
Health Hazard
Methyl chloroformate is highly toxic upon inhalation and upon ingestion. A concentration of 1 mg/liter (190 ppm) has been lethal in 10 minutes. It is corrosive and irritating to skin.
Fire Hazard
Methyl chloroformate is very dangerous when exposed to heat sources, sparks, flame, or oxidizers. Methyl chloroformate will react with water or steam to produce toxic and corrosive fumes. Vapors may travel to a source of ignition and flash back. Withdraw immediately in case of rising sound from venting safety device or any discoloration of tank due to fire. Toxic fumes of phosgene are produced when the material is heated to decomposition. Heat or steam should be avoided.
Flammability and Explosibility
Flammable
Chemical Reactivity
Reactivity with Water: Reacts slowly, evolving hydrogen chloride (hydrochloric acid). Reaction can be hazardous if water is hot; Reactivity with Common Materials: Corrodes rubber; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Flush with water, rinse with sodium bicarbonate or lime solution; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.
Safety Profile
Poison by ingestion,
inhalation, and intraperitoneal routes.
Moderately toxic by skin contact. Human
systemic effects by inhalation: conjunctiva
irritation and respiratory effects. Corrosive
to skin, eyes, and mucous membranes. Very
dangerous fire hazard when exposed to heat
sources, sparks, flame, or oxidzers. Reacts
with water or steam to produce toxic and
corrosive fumes. When heated to
decomposition it emits toxic fumes of Cl-,
methyl chloroformate, and phosgene.
Synthesis
Methyl chloroformate prepared by reacting methyl alcohol with phosgene.A side product (methyl carbonate) could be formed if the temperature is not kept rather low and phosgene is not used in excess:To a reaction flask fitted with a dropping-funnel, a tube to introduce the gaseous phosgene and an exit tube a 10 ml of methyl chloroformate is placed. The reaction flask is cooled to 0° C and the current of phosgene containing no chlorine is bubbled in. About one-third of reaction flask is filled with methanol from the dropping-funnel all at once. When the phosgene gas is no longer being absorbed additional portion of a fresh methanol is added to the reaction mixture. As soon as the reaction is complete, methyl chloroformate is transferred to a separatory funnel containing cold water. The heavier layer which separates from the aqueous layer is washed twice with cold water, dried over calcium chloride and fractionally distilled. The fraction passing over between 69-72 °C is collected. The yield of methyl chloroformate is about 70% of theory.The war gases chemistry and analysis, by M. Sartory, 102, 1939.
Potential Exposure
Used in synthesis of pharmaceuticals;
herbicides, plastics and other organic chemicals; as a solvent in the photographic industry; as a chemical intermediate in the production of other chemicals. In WWI it was
used as military tear-producing warfare agent.
Shipping
UN1238 Methyl chloroformate, Hazard class:
6.1; Labels: 6.1-Poison Inhalation Hazard, 3-Flammable
liquid, 8-Corrosive material Inhalation Hazard Zone A
Incompatibilities
May form explosive mixture with air.
Violent reaction with alkali metals; ethers. Incompatible
with strong acids; strong bases; alcohols, oxidizers,
dimethylsulfoxide; dimethyl formamide. Contact with water
or moisture produces corrosive and poisonous hydrogen
chloride gas, methanol and carbon monoxide. Corrodes
metals in the presence of moisture. Attacks some plastics,
rubber and coatings.
Waste Disposal
Consult with environmental
regulatory agencies for guidance on acceptable disposal
practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform to EPA regulations
governing storage, transportation, treatment, and waste
disposal
Check Digit Verification of cas no
The CAS Registry Mumber 79-22-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79-22:
(4*7)+(3*9)+(2*2)+(1*2)=61
61 % 10 = 1
So 79-22-1 is a valid CAS Registry Number.
InChI:InChI=1/C2H3ClO2/c1-5-2(3)4/h1H3
79-22-1Relevant articles and documents
-
Bailey,Di Pietro
, p. 179 (1978)
-
Synthesis of N-trifluoromethyl amides from carboxylic acids
Flavell, Robert R.,Liu, Jianbo,Parker, Matthew F. L.,Toste, F. Dean,Wang, Sinan,Wilson, David M.
supporting information, p. 2245 - 2255 (2021/08/12)
Found in biomolecules, pharmaceuticals, and agrochemicals, amide-containing molecules are ubiquitous in nature, and their derivatization represents a significant methodological goal in fluorine chemistry. Trifluoromethyl amides have emerged as important functional groups frequently found in pharmaceutical compounds. To date, there is no strategy for synthesizing N-trifluoromethyl amides from abundant organic carboxylic acid derivatives, which are ideal starting materials in amide synthesis. Here, we report the synthesis of N-trifluoromethyl amides from carboxylic acid halides and esters under mild conditions via isothiocyanates in the presence of silver fluoride at room temperature. Through this strategy, isothiocyanates are desulfurized with AgF, and then the formed derivative is acylated to afford N-trifluoromethyl amides, including previously inaccessible structures. This method shows broad scope, provides a platform for rapidly generating N-trifluoromethyl amides by virtue of the diversity and availability of both reaction partners, and should find application in the modification of advanced intermediates.
Discovery of (3-Benzyl-5-hydroxyphenyl)carbamates as new antitubercular agents with potent in vitro and in vivo efficacy
Cheng, Ya-Juan,Liu, Zhi-Yong,Liang, Hua-Ju,Fang, Cui-Ting,Zhang, Niu-Niu,Zhang, Tian-Yu,Yan, Ming
, (2019/06/07)
A series of 3-amino-5-benzylphenol derivatives were designed and synthesized. Among them, (3-benzyl-5-hydroxyphenyl)carbamates were found to exert good inhibitory activity against M. tuberculosis H37Ra, H37Rv and clinically isolated multidrug-resistant M. tuberculosis strains (MIC = 0.625-6.25 μg/mL). The privileged compounds 3i and 3l showed moderate cytotoxicity against cell line A549. Compound 3l also exhibited potent in vivo inhibitory activity on a mouse infection model via the oral administration. The results demonstrated 3-hydroxyphenylcarbamates as a class of new antitubercular agents with good potential.
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