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2,6-Dichloro-3,5-dimethoxyaniline

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Products Intro: Product Name:2,6-Dichloro-3,5-dimethoxybenzenamine
CAS:872509-56-3
Purity:98% Package:100G, 5KG, 25KG or as request Remarks:Commercial stage
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Products Intro: Product Name:2,6-dichloro-3,5-dimethoxyaniline
CAS:872509-56-3
Purity:98% Package:1kg;5kg;10kg;100kg
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Products Intro: Product Name:2,6-Dichloro-3,5-dimethoxyaniline
CAS:872509-56-3
Purity:98% Min. Package:1G;1KG;100KG
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Products Intro: Product Name:2,6-Dichloro-3,5-dimethoxyaniline
CAS:872509-56-3
Purity:99% Package:1KG,5KG,10KG
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Products Intro: Product Name:2,6-Dichloro-3,5-dimethoxyaniline
CAS:872509-56-3
Purity:0.98 Package:25KG;5KG;1KG Remarks:Mature product

2,6-Dichloro-3,5-dimethoxyaniline manufacturers

2,6-Dichloro-3,5-dimethoxyaniline Basic information
Product Name:2,6-Dichloro-3,5-dimethoxyaniline
Synonyms:2,6-Dichloro-3,5-dimethoxyaniline;2,6-Dichloro-3,5-dimethoxybenzenamine;Benzenamine, 2,6-dichloro-3,5-dimethoxy-;2,6-Dichloro-3,5-dimethoxy-phenylamine;157427;oro-3,5-dimethoxyaniL
CAS:872509-56-3
MF:C8H9Cl2NO2
MW:222.07
EINECS:
Product Categories:
Mol File:872509-56-3.mol
2,6-Dichloro-3,5-dimethoxyaniline Structure
2,6-Dichloro-3,5-dimethoxyaniline Chemical Properties
Boiling point 320℃
density 1.357
Fp 147℃
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka-0.13±0.10(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C8H9Cl2NO2/c1-12-4-3-5(13-2)7(10)8(11)6(4)9/h3H,11H2,1-2H3
InChIKeyLCQFHEIDCMPNAN-UHFFFAOYSA-N
SMILESC1(N)=C(Cl)C(OC)=CC(OC)=C1Cl
Safety Information
HS Code 2922299090
MSDS Information
2,6-Dichloro-3,5-dimethoxyaniline Usage And Synthesis
Chemical PropertiesWhite to off-white powder
Uses2,6-Dichloro-3,5-dimethoxyaniline is primarily used as an intermediate in the synthesis of pharmaceuticals.
Synthesis
N-(2,6-dichloro-3,5-dimethoxyphenyl)acetamide

943189-21-7

2,6-Dichloro-3,5-dimethoxyaniline

872509-56-3

N-(2,6-dichloro-3,5-dimethoxyphenyl)acetamide (34.5 g, 131 mmol) was used as a raw material and dissolved in ethanol (600 mL). Subsequently, 2N aqueous potassium hydroxide solution (400 mL) was added to this solution to obtain the reaction mixture. The reaction mixture was heated to 90°C and stirred, and the reaction was kept at reflux for 2 days. Upon completion of the reaction, the mixture was cooled to room temperature, then cooled to 0 °C in an ice water bath and stirring was continued for 1 hour. The precipitated solid was collected by filtration, washed with cold ethanol/water (1:1, v/v) mixed solvent and dried to give 2,6-dichloro-3,5-dimethoxyaniline (22.1 g, 76% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d5): δ 6.21 (s, 1H), 5.40 (s, 2H), 3.83 (s, 6H).

References[1] Journal of Medicinal Chemistry, 2011, vol. 54, # 20, p. 7066 - 7083
[2] Patent: US2016/145240, 2016, A1. Location in patent: Paragraph 0098; 0099
[3] Patent: WO2016/164703, 2016, A1. Location in patent: Page/Page column 36
[4] Patent: WO2016/164754, 2016, A1. Location in patent: Page/Page column 33
[5] Patent: WO2006/420, 2006, A1. Location in patent: Page/Page column 157
2,6-Dichloro-3,5-dimethoxyaniline Preparation Products And Raw materials
Raw materialsEthanol-->N-(2,6-dichloro-3,5-dimethoxyphenyl)acetamide-->Water-->Potassium hydroxide
Preparation Products2,4-dichloro-3-isocyanato-1,5-dimethoxybenzene
Tag:2,6-Dichloro-3,5-dimethoxyaniline(872509-56-3) Related Product Information
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