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CAS No.: | 58993-79-6 |
---|---|
Name: | (R)-2-(4-Methoxyphenyl)-1-methylethanamine |
Article Data: | 25 |
Molecular Structure: | |
Formula: | C10H15NO |
Molecular Weight: | 165.235 |
Synonyms: | Benzeneethanamine,4-methoxy-a-methyl-, (R)-;(-)-p-Methoxyamphetamine;(R)-(-)-2-(4-Methoxyphenyl)-1-methylethylamine;(R)-2-(4-Methoxyphenyl)-1-methyl-ethylamine;l-4-Methoxyamphetamine; |
Density: | 0.99 g/cm3 |
Boiling Point: | 258.2 °C at 760 mmHg |
Flash Point: | 107.5 °C |
PSA: | 35.25000 |
LogP: | 2.28520 |
(R)-1-(4-methoxyphenyl)-N-((R)-1-phenylethyl)propan-2-amine
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol at 40℃; for 24h; | 99.8% |
With palladium 10% on activated carbon; hydrogen In methanol at 45℃; under 15201 Torr; for 8h; Autoclave; | 94% |
With palladium 10% on activated carbon at 50℃; under 37503.8 Torr; for 1h; |
4-methoxybenzyl methyl ketone
2-Pentanone
A
(R)‐2‐aminopentane
B
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
With Candida boidinii formate dehydrogenase; pyridoxal 5'-phosphate; Aspergillus terreus ω-trans aminase; Lysinibacillus fusiformis leucine dehydrogenase; ammonium formate; nicotinamide adenine dinucleotide In aq. buffer at 30℃; for 24h; pH=8.8; Catalytic behavior; Green chemistry; Enzymatic reaction; | A 99.7% B 99.4% |
4-methoxybenzyl methyl ketone
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
With glucose dehydrogenase; D-Alanine; D-glucose; ω-transaminase ATA-117; pyridoxal 5'-phosphate; nicotinamide adenine dinucleotide; lactate dehydrogenase In dimethyl sulfoxide at 30℃; for 24h; pH=7; aq. phosphate buffer; Enzymatic reaction; optical yield given as %ee; stereoselective reaction; | 99% |
With pyridoxal 5'-phosphate; amine transaminase TA-P2-B01; isopropylamine In aq. phosphate buffer at 30℃; for 24h; pH=7.5; Reagent/catalyst; Enzymatic reaction; enantioselective reaction; | 86% |
With Cb-FDH formate dehydrogenase (variant) from Candida boidinii; Rs-PhAmDH amine dehydrogenase variant from the phenylalanine dehydrogenase from Rhodoccoccus species; NAD; ammonium formate In water at 30℃; for 24h; pH=8.5; Reagent/catalyst; Enzymatic reaction; stereoselective reaction; | 82% |
(4R,5S)-5-(4-methoxyphenyl)-4-methyloxazolidin-2-one
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol at 20℃; for 1h; atmospheric pressure; | 91% |
(R)-N-[2-(4'-methoxyphenyl)-1-methylethyl]-2-methoxyacetamide
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
With water; potassium hydroxide Reflux; optical yield given as %ee; | 70% |
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
With hydrogenchloride; D-sorbitol; choline chloride In water at 25℃; for 3h; | 60% |
ethyl 2-methoxyacetate
2-amino-1-(4-methyoxyphenyl)propane
A
(R)-N-[2-(4'-methoxyphenyl)-1-methylethyl]-2-methoxyacetamide
B
(S)-2-(4-methoxy-phenyl)-1-methyl-ethylamine
C
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
With Candida antartica lipase B; triethylamine In n-heptane at 50℃; for 25h; Inert atmosphere; Enzymatic reaction; optical yield given as %ee; | A 49% B 40% C n/a |
With Candida antartica lipase B; triethylamine In n-heptane at 35℃; for 1.5h; Inert atmosphere; Enzymatic reaction; optical yield given as %ee; | A 38% B n/a C n/a |
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol; water |
1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene
A
(S)-2-(4-methoxy-phenyl)-1-methyl-ethylamine
B
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
Stage #1: 1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene With lithium aluminium tetrahydride In diethyl ether for 2h; Reduction; Heating; Stage #2: With Candida antarctica lipase B; ethyl acetate; triethylamine at 30℃; for 4h; racemate resolution; Title compound not separated from byproducts; |
(R)-N-[1-(o-methoxyphenyl)propan-2-yl]ethanamide
(R)-(-)-p-methoxyamphetamine
Conditions | Yield |
---|---|
With potassium hydroxide Hydrolysis; Heating; |
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The systematic name of (R)-2-(4-Methoxyphenyl)-1-methylethanamine is (2R)-1-(4-methoxyphenyl)propan-2-amine. With the CAS registry number 58993-79-6, it is also named as Benzeneethanamine,4-methoxy-a-methyl-, (R)-. The product's category is tamsulosin. Moreover, its molecular formula is C10H15NO and its molecular weight is 165.23.
The other characteristics of (R)-2-(4-Methoxyphenyl)-1-methylethanamine can be summarized as: (1)ACD/LogP: 1.72; (2)# of Rule of 5 Violations: 0; (3)H bond acceptors: 2; (4)H bond donors: 2; (5)Freely Rotating Bonds: 4; (6)Nominal mass: 165; (7)Average mass: 165.2322; (8)Monoisotopic mass: 165.115364; (9)Polar Surface Area: 12.47 Å2; (10)Index of Refraction: 1.518; (11)Molar Refractivity: 50.6 cm3; (12)Molar Volume: 166.8 cm3; (13)Polarizability: 20.06×10-24cm3; (14)Surface Tension: 35.3 dyne/cm; (15)Density: 0.99 g/cm3; (16)Flash Point: 107.5 °C; (17)Enthalpy of Vaporization: 49.58 kJ/mol; (18)Boiling Point: 258.2 °C at 760 mmHg; (19)Vapour Pressure: 0.0139 mmHg at 25 °C.
People can use the following data to convert to the molecule structure.
(1)SMILES:O(c1ccc(cc1)C[C@H](N)C)C
(2)InChI:InChI=1/C10H15NO/c1-8(11)7-9-3-5-10(12-2)6-4-9/h3-6,8H,7,11H2,1-2H3/t8-/m1/s1
(3)InChIKey:NEGYEDYHPHMHGK-MRVPVSSYBI
(4)Std. InChI:InChI=1S/C10H15NO/c1-8(11)7-9-3-5-10(12-2)6-4-9/h3-6,8H,7,11H2,1-2H3/t8-/m1/s1
(5)Std. InChIKey:NEGYEDYHPHMHGK-MRVPVSSYSA-N