methanol
3-Vinylbicyclobutane-1-carbonitrile
A
sodium methylate
B
3-(2-Methoxyethylidene)cyclobutane-1-carbonitrile
C
Z-3-vinyl-3-methoxycyclobutane-1-carbonitrile
Conditions | Yield |
---|---|
With perchloric acid at 20℃; for 5h; Yields of byproduct given; | A n/a B 35% C n/a |
diazomethane
Methyl formate
2-(carboxymethyl)-4-methoxybenzoic acid
B
sodium methylate
Conditions | Yield |
---|---|
With diethyl ether Erwaermen des danach isolierten Reaktionsprodukts mit konz. wss.Salzsaeure; |
Conditions | Yield |
---|---|
With [Ru4(μ-H)4(CO)12] at 25℃; Rate constant; Equilibrium constant; various carbonyl hydride complexes of Fe, Ru, and Os; | |
With sodium hydroxide; water at 20℃; Equilibrium constant; | |
With sodium hydroxide |
Conditions | Yield |
---|---|
at 210 - 240℃; im Vakuum; | |
210-280°C; | |
210-280°C; | |
210-280°C; |
methanol
bis-methoxycarbonyl-methanide
A
sodium methylate
B
malonic acid dimethyl ester
Conditions | Yield |
---|---|
at 25℃; Equilibrium constant; |
methanol
ethyl cyanoacetate anion
A
sodium methylate
B
ethyl 2-cyanoacetate
Conditions | Yield |
---|---|
at 25℃; Equilibrium constant; |
methanol
4-nitrobenzyl cyanide anion
A
sodium methylate
B
4-Nitrophenylacetonitrile
Conditions | Yield |
---|---|
at 25℃; Equilibrium constant; |
methanol
p-cyano-phenyl-acetonitrile anion
A
4-(cyanomethyl)benzonitrile
B
sodium methylate
Conditions | Yield |
---|---|
at 25℃; Equilibrium constant; |
methanol
2-cyanobenzyl cyanide anion
A
(2-cyanophenyl)acetonitrile
B
sodium methylate
Conditions | Yield |
---|---|
at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
In methanol; dimethyl sulfoxide at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
In methanol; dimethyl sulfoxide at 25℃; for 0.0166667h; Rate constant; Equilibrium constant; |
2,6-Di-tert-butyl-2-methoxy-2H-thiopyran
A
sodium methylate
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
2,6-Di-tert-butyl-4-methoxy-4H-thiopyran
A
sodium methylate
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
2,6-Di-tert-butyl-4-methoxy-4-methyl-4H-thiopyran
A
sodium methylate
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
2,4,6-Tri-tert-butyl-4-methoxy-4H-thiopyran
A
sodium methylate
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
2,4,6-Tri-tert-butyl-2-methoxy-2H-thiopyran
A
sodium methylate
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
4-Methoxy-4-methyl-2,6-diphenyl-4H-pyran
B
sodium methylate
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
2-Methoxy-4-methyl-2,6-diphenyl-2H-pyran
B
sodium methylate
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
4-tert-Butyl-2-methoxy-2,6-diphenyl-2H-pyran
A
sodium methylate
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
Sodium 1,1-dimethoxy-2,4,6-trinitrocyclohexadienate-2,5
A
sodium methylate
B
1-methoxy-2,4,6-trinitrobenzene
Conditions | Yield |
---|---|
In methanol at 25℃; various initial concetration also with potasium salt, var. slovents and additive; |
A
sodium methylate
B
1,3-dinitro-4-phenanthryl methyl ether
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
In methanol; dimethyl sulfoxide at 25℃; Rate constant; Equilibrium constant; |
Conditions | Yield |
---|---|
In methanol; dimethyl sulfoxide at 25℃; Equilibrium constant; |
A
5-chloro-4-methoxy-1,3-dinitrobenzene
B
sodium methylate
Conditions | Yield |
---|---|
With (decomposition) In methanol at 25℃; Equilibrium constant; Rate constant; | |
With (decomposition); barium(II) chloride In methanol at 25℃; Equilibrium constant; other catalyst; |
Conditions | Yield |
---|---|
With (decomposition) In methanol at 25℃; Equilibrium constant; Rate constant; |
Conditions | Yield |
---|---|
In methanol at 25℃; Equilibrium constant; Kinetics; | |
With (decomposition); barium(II) chloride In methanol at 25℃; Equilibrium constant; | |
With (decomposition) In methanol at 25℃; Equilibrium constant; Rate constant; |
A
2-methoxy-3,5-dinitro-benzoic acid methyl ester
B
sodium methylate
Conditions | Yield |
---|---|
With (decomposition) In methanol at 25℃; Equilibrium constant; Rate constant; | |
With (decomposition); barium(II) chloride In methanol at 25℃; Equilibrium constant; Rate constant; other catalyst; |
1,2-dibromo-3-methoxypropane
A
sodium methylate
B
propargyl alcohol methyl ether
Conditions | Yield |
---|---|
at 230 - 270℃; |
Conditions | Yield |
---|---|
In methanol for 20h; Heating / reflux; | 100% |
With 1,4-dioxane; methanol | |
In methanol Reflux; | 8.8 g |
2-chloro-4,6-dimethylnicotinonitrile
sodium methylate
3-cyano-4,6-dimethyl-2-methoxypyridine
Conditions | Yield |
---|---|
In methanol for 1h; | 100% |
In methanol at 0℃; for 10h; | 99% |
In methanol at 60℃; for 4h; | 65% |
With methanol |
sodium methylate
4-picolylchloride hydrochloride
4-(methoxymethyl)pyridine
Conditions | Yield |
---|---|
In methanol at 90℃; for 12h; | 100% |
With methanol | |
for 4h; Inert atmosphere; Reflux; |
Conditions | Yield |
---|---|
With N-Bromosuccinimide In methanol for 0.166667h; Heating; | 100% |
With methanol; bromine |
Conditions | Yield |
---|---|
In methanol at 60℃; for 24h; | 100% |
In toluene for 24h; |
3,4-dichlorotetrahydrothiophene-1,1-dioxide
sodium methylate
trans-3,4-Dimethoxythiolane-1,1-dioxide
Conditions | Yield |
---|---|
In methanol at 58.9 - 63.9℃; | 100% |
Conditions | Yield |
---|---|
In methanol for 14h; Product distribution; Heating; | 100% |
In methanol for 14h; Heating; Yield given; |
6-oxabicyclo[3.2.1]oct-3-en-7-one
sodium methylate
cis-methyl 5-hydroxycyclohex-3-enecarboxylate
Conditions | Yield |
---|---|
In methanol at 25℃; for 12h; | 100% |
Methyl 3,4-anhydro-2,6-dideoxy-α-L-ribo-hexopyranoside
sodium methylate
methyl α-L-oleandropyranoside
Conditions | Yield |
---|---|
In methanol for 18h; Heating; | 100% |
2,4,5,6-Tetrafluoro-1,3-dinitrobenzene
sodium methylate
Conditions | Yield |
---|---|
In methanol Ambient temperature; | 100% |
dichlorure de l'acide N-(phenylmethyl) carbonimidique
sodium methylate
methyl N-benzylchloroformimidate
Conditions | Yield |
---|---|
In diethyl ether for 48h; Heating; | 100% |
In diethyl ether at 25℃; |
1,2,3,4-Tetrafluorodibenz<1,4>-oxazepin-11-(10H)-one
sodium methylate
3-methoxy-1,2,4-trifluorobenz<1,4>oxazepin-11(10H)-one
Conditions | Yield |
---|---|
In methanol for 1h; Heating; | 100% |
sodium methylate
5-chloro-6-dichloromethyl-3-phenyl-as-triazine
6-Dimethoxymethyl-5-methoxy-3-phenyl-[1,2,4]triazine
Conditions | Yield |
---|---|
In methanol Heating; | 100% |
sodium methylate
<(3R)-5α>-2',2'-Dichlorospiro-3'-one
<(3S)-5α>-2',2'-dimethoxyspiro-3'-one
Conditions | Yield |
---|---|
In methanol for 0.0833333h; Mechanism; Ambient temperature; | 100% |
In methanol for 0.0833333h; Ambient temperature; | 100% |
sodium methylate
4,4'-Bis(brommethyl)-1,1'-binaphthalin
4,4'-Bis(methoxymethyl)-1,1'-binaphthalin
Conditions | Yield |
---|---|
In methanol for 24h; Heating; | 100% |
sodium methylate
5-tert-butylamino-3,6-dichloro-1,2,4-triazine
3-methoxy-5-tert-butylamino-6-chloro-1,2,4-triazine
Conditions | Yield |
---|---|
In methanol Ambient temperature; | 100% |
sodium methylate
2-chloro-6-methylsulphenylpyridine
2-methoxy-6-(methylthio)pyridine
Conditions | Yield |
---|---|
In methanol for 20h; Heating; | 100% |
sodium methylate
1,1-dimethoxy-1-phenyl-2-propanone
Conditions | Yield |
---|---|
In methanol for 0.5h; Ambient temperature; | 100% |
sodium methylate
(1-chloro-1-phenyl-2-propylidene)cyclohexylamine
methyl N-cyclohexyl-3-phenylpropanimidate
Conditions | Yield |
---|---|
In tetrahydrofuran for 22h; Heating; | 100% |
sodium methylate
9,11-dihydro-α-ethyl-9-oxoindolizino<1,2-b>quinoline-7-acetic acid, ethyl ester
9,11-dihydro-α-ethyl-9-oxoindolizino<1,2-b>quinoline-7-acetic acid, methyl ester
Conditions | Yield |
---|---|
In methanol | 100% |
sodium methylate
4-Chlorocarbonylmethyl-2-difluoromethyl-6-trifluoromethyl-pyridine-3,5-dicarboxylic acid dimethyl ester
dimethyl 2-(difluoromethyl)-4-(2-methoxy-2-oxoethyl)-6-(trifluoromethyl)-3,5-pyridinedicarboxylate
Conditions | Yield |
---|---|
In methanol for 1h; | 100% |
sodium methylate
Formic acid (1R,3aS,3bR,5aS,6aR,8R,8aR,9aS,9bS,11aR)-8-chloro-1-((R)-1,5-dimethyl-hexyl)-9a,11a-dimethyl-7-oxo-octadecahydro-cyclobuta[h]cyclopenta[a]phenanthren-6a-yl ester
(1R,3aS,3bR,5aS,6aR,8R,8aR,9aS,9bS,11aR)-8-Chloro-1-((R)-1,5-dimethyl-hexyl)-6a-methoxy-9a,11a-dimethyl-octadecahydro-cyclobuta[h]cyclopenta[a]phenanthren-7-one
Conditions | Yield |
---|---|
In tetrahydrofuran; methanol Ambient temperature; | 100% |
sodium methylate
Acetic acid (1R,3aS,3bR,5aS,6aR,8R,8aR,9aS,9bS,11aR)-8-chloro-1-((R)-1,5-dimethyl-hexyl)-9a,11a-dimethyl-7-oxo-octadecahydro-cyclobuta[h]cyclopenta[a]phenanthren-6a-yl ester
(1R,3aS,3bR,5aS,6aR,8R,8aR,9aS,9bS,11aR)-8-Chloro-1-((R)-1,5-dimethyl-hexyl)-6a-methoxy-9a,11a-dimethyl-octadecahydro-cyclobuta[h]cyclopenta[a]phenanthren-7-one
Conditions | Yield |
---|---|
In tetrahydrofuran; methanol Ambient temperature; | 100% |
In methanol Heating; |
sodium methylate
peracetylated α-glycosyl nitrate 2-azido-2-deoxy-D-galactopyranose
(2R,3R,4R,5R,6R)-5-azido-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4-diol
Conditions | Yield |
---|---|
100% |
sodium methylate
1,1-Dimethylazetidinium Perchlorate
3-(Dimethylamino)-1-propyl Methyl Ether
Conditions | Yield |
---|---|
In methanol at 20℃; Rate constant; Product distribution; various temperatures; | 100% |
sodium methylate
Benzoic acid (1R,3aS,3bR,5aS,6aR,8R,8aR,9aS,9bS,11aR)-8-chloro-1-((R)-1,5-dimethyl-hexyl)-9a,11a-dimethyl-7-oxo-octadecahydro-cyclobuta[h]cyclopenta[a]phenanthren-6a-yl ester
(1R,3aS,3bR,5aS,6aR,8R,8aR,9aS,9bS,11aR)-8-Chloro-1-((R)-1,5-dimethyl-hexyl)-6a-methoxy-9a,11a-dimethyl-octadecahydro-cyclobuta[h]cyclopenta[a]phenanthren-7-one
Conditions | Yield |
---|---|
In tetrahydrofuran; methanol Ambient temperature; | 100% |
sodium methylate
Conditions | Yield |
---|---|
In methanol at 0℃; for 0.25h; | 100% |
sodium methylate
(S)-5-tosyloxypentan-4-olide
3-(S)-oxiranyl-propionic acid methyl ester
Conditions | Yield |
---|---|
In methanol for 0.333333h; Ambient temperature; | 100% |
In methanol at 20℃; for 3h; Inert atmosphere; | 97% |
In methanol at 20℃; for 1.5h; | 53% |
sodium methylate
2-(1,2,2,5,5-Pentamethyl-3-oxy-2,5-dihydro-1H-imidazol-4-yl)-1-phenyl-ethanone
Conditions | Yield |
---|---|
With semicarbazide hydrochloride In methanol for 2.5h; Heating; | 100% |
sodium methylate
3-[1-Pyridin-2-yl-meth-(E)-ylidene]-3H-benzofuran-2-one
(E)-2-(2-Hydroxy-phenyl)-3-pyridin-2-yl-acrylic acid methyl ester
Conditions | Yield |
---|---|
In methanol for 2h; Ambient temperature; | 100% |
Molecular structure of Sodium methanolate (CAS NO.124-41-4) is:
Product Name: Sodium methanolate
CAS Registry Number: 124-41-4
IUPAC Name:&nbsp;sodium methanolate
Molecular Weight: 54.02369 [g/mol]
Molecular Formula: CH3NaO
H-Bond Donor: 0
H-Bond Acceptor: 1
EINECS: 204-699-5
Melting Point: -98 °C
Flash Point: 11.1 °C
Enthalpy of Vaporization: 35.21 kJ/mol
Boiling Point: 48.1 °C at 760 mmHg
Vapour Pressure: 265 mmHg at 25 °C
Density: 0.97 g/mL at 20°C
Refractive index: 1.3700
Storage temp.: Flammables area
Water Solubility: reacts
Sensitive Moisture: Sensitive
Stability: Stability Highly flammable. Reacts violently with water. Keep container dry. Incompatible with water, acids, chlorinated solvents.
Product Categories: Organics;Classes of Metal Compounds;Na (Sodium) Compounds (excluding simple sodium salts);Typical Metal Compounds
Sodium methanolate (CAS NO.124-41-4) has very important use in both organic synthesis and industrial applications:
Organic synthesis: It&nbsp;is a routine base in organic chemistry, applicable to the synthesis of numerous compounds, ranging from pharmaceuticals to agrichemicals. As a base, it is employed in dehydrohalogenations and aldol condensations. It is also a nucleophile for the production of methyl ethers.
Industrial applications: It is used as an initiator of an anionic addition polymerization with ethylene oxide, forming a polyether with high molecular weight. Biodiesel is prepared from vegetable oils and animal fats, that is, fatty acid triglycerides, by transesterification with methanol to give fatty acid methyl esters (FAMEs). This transformation is catalyzed by sodium methoxide.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rat | LD50 | oral | 2037mg/kg (2037mg/kg) | SENSE ORGANS AND SPECIAL SENSES: CHROMODACYRORREA: EYE BEHAVIORAL: ATAXIA LUNGS, THORAX, OR RESPIRATION: DYSPNEA | National Technical Information Service. Vol. OTS0555267, |
Statements: 11-23/24/25-34-39/23/24/25-36/38-14-36/37/38
R11:Highly flammable.
R23/24/25:Toxic by inhalation, in contact with skin and if swallowed.
R34:Causes burns.
R39:Danger of very serious irreversible effects.
R36/38:Irritating to eyes and skin.
R14 :Reacts violently with water.
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 8-16-26-43-45-7-36/37-7/8-36/37/39
S8:Keep container dry.
S16:Keep away from sources of ignition.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.&nbsp;<br /> S36/37:Wear suitable protective clothing and gloves.
S7/8:Keep container tightly closed and dry.&nbsp;<br /> S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
RIDADR: UN 1431 4.2/PG 2
WGK Germany: 1
RTECS: PC3570000
F: 9-21
TSCA: Yes
HazardClass: 4.2
PackingGroup: II
HS Code: 29051900
Sodium methanolate , its cas register number is 124-41-4. It also can be called Sodium methoxide ; Sodium methylate .It is a colorless cloudy white liquid consisting of sodium methylate, a solid, dissolved in methyl alcohol.It is&nbsp;highly flammable and reacts with water to produce a mixed solution of sodium hydroxide and methyl alcohol.
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