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2-METHOXY-6-METHYLANILINE

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Products Intro: Product Name:2-METHOXY-6-METHYLANILINE
CAS:50868-73-0
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CAS:50868-73-0
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CAS:50868-73-0
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2-METHOXY-6-METHYLANILINE manufacturers

2-METHOXY-6-METHYLANILINE Basic information
Product Name:2-METHOXY-6-METHYLANILINE
Synonyms:6-METHYL-O-ANISIDINE;2-METHOXY-6-METHYLANILINE;2-Methoxy-6-methyl-phenylamine;2-Amino-1-methoxy-3-methylbenzene;6-Methoxy-o-toluidine;2-Methoxy-6-methylbenzenamine;2-Methyl-6-methoxyaniline;6-Methoxy-2-methylaniline
CAS:50868-73-0
MF:C8H11NO
MW:137.18
EINECS:
Product Categories:Amines;Building Blocks;C8;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks
Mol File:50868-73-0.mol
2-METHOXY-6-METHYLANILINE Structure
2-METHOXY-6-METHYLANILINE Chemical Properties
Melting point 26-29 °C (lit.)
Boiling point 62 °C/0.15 mmHg (lit.)
density 1.0630 (rough estimate)
refractive index 1.5647 (estimate)
Fp >230 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform (Slightly), Methanol (Sparingly)
pka4.39±0.10(Predicted)
form Solid
color Clear Brown Oil to Pale Red to Dark Red
InChIInChI=1S/C8H11NO/c1-6-4-3-5-7(10-2)8(6)9/h3-5H,9H2,1-2H3
InChIKeyHKOJYPPTIPJZAZ-UHFFFAOYSA-N
SMILESC1(N)=C(C)C=CC=C1OC
CAS DataBase Reference50868-73-0
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 26-37/39
WGK Germany 3
HS Code 2922290090
Storage Class10 - Combustible liquids
Hazard ClassificationsAcute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
2-METHOXY-6-METHYLANILINE Usage And Synthesis
Uses2-Methoxy-6-methylaniline may be used in the synthesis of 7-methoxy-1H-indazole, an inhibitor of nitric oxide synthase.
Synthesis
3-Methyl-2-nitroanisole

5345-42-6

2-METHOXY-6-METHYLANILINE

50868-73-0

General procedure for the synthesis of 2-methoxy-6-methylaniline from 3-methyl-2-nitroanisole: Step A2; a) Preparation of intermediate 3: 1-methoxy-3-methyl-2-nitrobenzene (25 g, 149.7 mmol) was dissolved in ethanol (100 ml). 10% palladium/carbon catalyst (2.5 g) was added and the reaction mixture was subjected to hydrogenation at room temperature for 24 hours. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration. The filtrate was concentrated under reduced pressure to give Intermediate 3 in a yield of 20.02 g (97% yield). The structure of intermediate 3 was confirmed by CI-MS with a molecular ion peak of 138 ([M + H]+).

References[1] New Journal of Chemistry, 2006, vol. 30, # 2, p. 168 - 176
[2] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 6, p. 3309 - 3320
[3] Organic letters, 2000, vol. 2, # 3, p. 277 - 280
[4] Patent: WO2006/15985, 2006, A1. Location in patent: Page/Page column 54-55
[5] Journal of the Chemical Society, 1926, p. 1425
2-METHOXY-6-METHYLANILINE Preparation Products And Raw materials
Raw materials3-Methyl-2-nitroanisole-->Ethanol-->Hydrogen
Preparation Products2-Methoxy-6-methylbenzoic acid
Tag:2-METHOXY-6-METHYLANILINE(50868-73-0) Related Product Information
Disperse Red 86 3-METHOXY-2-NITROBENZOIC ACID Methyl 2-amino-3,4,5-trimethoxybenzoate Actinomycin D DISPERSE VIOLET 26 3-Methyl-2-nitroanisole MEDINOTERB ACETATE METHYL 3-METHOXY-2-NITROBENZOATE Methyl 2-nitro-3,4,5-trimethoxybenzoate Disperse Red 11 2-AMINO-3,4,5-TRIMETHOXYBENZOIC ACID 3-Methoxy-2-nitrobenzaldehyde 5-Methoxy-2-methylaniline 4-Chloro-2-methoxy-N-methylaniline 96% 2-Methyl-4-methoxybenzenamine 2-Methoxy-4-methylaniline, HCl N-METHYL-P-ANISIDINE 3-METHOXY-N-METHYLANILINE

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