318183
Methyl sulfate sodium salt
Synonym(s):
Monomethyl ester sulfuric acid sodium salt, Sodium methyl sulfate
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About This Item
Linear Formula:
CH3OSO3Na
CAS Number:
Molecular Weight:
134.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
form
powder
Quality Level
impurities
<3% methanol
<5% water
mp
210 °C (lit.)
SMILES string
[Na+].COS([O-])(=O)=O
InChI
1S/CH4O4S.Na/c1-5-6(2,3)4;/h1H3,(H,2,3,4);/q;+1/p-1
InChI key
DZXBHDRHRFLQCJ-UHFFFAOYSA-M
Application
Methyl sulfate sodium salt can be used to synthesize:
- Methylsulfate anion based 1,3,4-trialkyl-1,2,3-triazolium ionic liquids for use in Morita–Baylis–Hillman reaction.
- Anisole by reacting with phenol.
- Hydroxyanilino quinolines for use as RET kinase inhibitors.
Reactant or reagent involved in:
- Studying lamellar structure formation in hybrid nanomaterials created by miniemulsion
- EPR studies of radical ions radiolytically generated from ionic liquids, used as a reference
- Micellular studies specifically the rate-retarding effects on hydrolysis of substituted 1-benzoyl-1,2,4-triazoles and self-assembly / microstructure of mixed micelles
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of anisole from phenol and sodium methyl sulfate, a byproduct from synthesis of medicine intermediates
Guoping W, et al.
Petrochemical Technology, 45(11), 1337-1337 (2016)
Synthesis of new triazolium-based ionic liquids and their use in the Morita-Baylis-Hillman reaction
F Alioune, et al.
Tetrahedron Letters, 56(36), 5128-5131 (2015)
The discovery of substituted 4-(3-hydroxyanilino)-quinolines as potent RET kinase inhibitors
Robinett R G, et al.
Bioorganic & Medicinal Chemistry Letters, 17(21), 5886-5893 (2007)
Dean Kirson et al.
The Journal of pharmacology and experimental therapeutics, 364(1), 70-76 (2017-11-10)
The amino acid taurine is an endogenous ligand acting on glycine receptors (GlyRs), which is released by astrocytes in many brain regions, such as the nucleus accumbens and prefrontal cortex. Taurine is a partial agonist with an efficacy significantly lower
Jung Su Park et al.
Science (New York, N.Y.), 329(5997), 1324-1327 (2010-09-11)
Ion binding often mediates electron transfer in biological systems as a cofactor strategy, either as a promoter or as an inhibitor. However, it has rarely, if ever, been exploited for that purpose in synthetic host-guest assemblies. We report here that
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