318183
Methyl sulfate sodium salt
Synonyma:
Monomethyl ester sulfuric acid sodium salt, Sodium methyl sulfate
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About This Item
Lineární vzorec:
CH3OSO3Na
Číslo CAS:
Molekulová hmotnost:
134.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Doporučené produkty
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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Zákazníci si také prohlíželi
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)
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)
V Chatsudthipong et al.
The Journal of pharmacology and experimental therapeutics, 288(3), 993-1001 (1999-02-23)
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Carbohydrate research, 344(1), 21-28 (2008-11-11)
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M A Sallam et al.
Carbohydrate research, 330(1), 53-63 (2001-02-24)
Dehydration of 4-(D-galacto-pentitol-1-yl)-2-phenyl-2H-1,2,3-triazole with 20% methanolic sulfuric acid afforded the anomeric pairs of nucleosides, 4-(alpha-D-lyxopyranosyl)-2-phenyl-2H-1,2,3-triazole (major component) and its beta-anomer, as well as 4-(alpha-D-lyxofuranosyl)-2H-1,2,3-triazole and its beta-anomer. The four anomeric C-nucleosides were separated by chromatography, and their structure and anomeric
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