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3,5-Dimethylanisole

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Company Name: Shanghai Fengtian Biotechnology Co., Ltd  Gold
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Company Name: Yuzhou Enthalpy Carbon Pharmaceutical Technology Co. LTD  Gold
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Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
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3,5-Dimethylanisole manufacturers

3,5-Dimethylanisole Basic information
Application
Product Name:3,5-Dimethylanisole
Synonyms:1,3-DIMETHYL-5-METHOXYBENZENE;3,5-DIMETHYLANISOLE;5-METHOXY-M-XYLENE;SPECS AC-509/25002099;3,5-Dimethylanisol;Anisole, 3,5-dimethyl;Benzene, 1-methoxy-3,5-dimethyl-;3,5-DIMETHYLANISOLE, 99+%
CAS:874-63-5
MF:C9H12O
MW:136.19
EINECS:212-865-3
Product Categories:Aromatic Ethers;Anisoles, Alkyloxy Compounds & Phenylacetates;Ethers;Organic Building Blocks;Oxygen Compounds
Mol File:874-63-5.mol
3,5-Dimethylanisole Structure
3,5-Dimethylanisole Chemical Properties
Boiling point 193 °C (lit.)
density 0.963 g/mL at 25 °C (lit.)
refractive index n20/D 1.512(lit.)
Fp 150 °F
storage temp. Sealed in dry,Room Temperature
form Liquid
color Clear colorless to light yellow
BRN 2040905
InChIInChI=1S/C9H12O/c1-7-4-8(2)6-9(5-7)10-3/h4-6H,1-3H3
InChIKeyJCHJBEZBHANKGA-UHFFFAOYSA-N
SMILESC1(OC)=CC(C)=CC(C)=C1
CAS DataBase Reference874-63-5(CAS DataBase Reference)
NIST Chemistry Reference3,5-Dimethylanisole(874-63-5)
Safety Information
Safety Statements 24/25
RIDADR 3271
WGK Germany 3
HS Code 29093090
Storage Class10 - Combustible liquids
MSDS Information
ProviderLanguage
3,5-Dimethylanisole English
SigmaAldrich English
ACROS English
ALFA English
3,5-Dimethylanisole Usage And Synthesis
Application3,5-Dimethylanisole is an ether organic compound that can be used as an organic intermediate.
Chemical Propertiesclear colourless to light yellow liquid
Synthesis
3,5-Dimethylphenol

108-68-9

Iodomethane

74-88-4

3,5-Dimethylanisole

874-63-5

3,5-Dimethylphenol (10 g, 0.082 mol) and anhydrous potassium carbonate (34 g, 0.25 mol) were added to N,N-dimethylformamide (DMF, 150 mL), and methyl iodide (12.8 g, 0.090 mol) was added slowly and dropwise under cooling in an ice bath. The reaction mixture was stirred at room temperature overnight. After completion of the reaction, water was added to the system and extracted with ethyl acetate. The organic phase was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by silica gel column chromatography afforded 3,5-dimethylanisole (10 g, 90% yield).1H NMR (400 MHz, CDCl3) δ: 6.60 (s, 1H), 6.53 (s, 2H), 3.77 (s, 3H), 2.29 (s, 6H).

References[1] Chemical Communications, 2011, vol. 47, # 25, p. 7218 - 7220
[2] Chemistry - An Asian Journal, 2016, vol. 11, # 22, p. 3267 - 3274
[3] Patent: EP2845854, 2015, A1. Location in patent: Paragraph 0101-0102
[4] Patent: US2015/133538, 2015, A1. Location in patent: Paragraph 0208-0211; 0232-0235; 0337-0340
[5] Patent: US2009/270469, 2009, A1. Location in patent: Page/Page column 28
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