2,6-Dimethyl-L-tyrosine supplier

Name
2,6-Dimethyl-L-tyrosine
EINECS
CAS No. 123715-02-6
Article Data9
CAS DataBase
Density 1.242 g/cm³
Solubility
Melting Point 239-240 °C (decomp)
Formula C₁₁H₁₅NO₃
Boiling Point 412.758 °C at 760 mmHg
Molecular Weight 209.245
Flash Point 203.429 °C
Transport Information
Appearance
Safety
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms L-2',6'-Dimethyltyrosine;2,6-Dimethyl-L-tyrosine;(S)-2-Amino-3-(4-hydroxy-2,6-dimethylphenyl)propionic acid;
PSA 83.55000
LogP 1.66370

Synthetic route

: 1185756-58-4
C44H50N2O8

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With hydrogen iodide for 3h; Reflux;	100%

: C21H30N2O4S

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With lithium hydroxide In tetrahydrofuran; water at 0℃; for 3h;	94.8%

: O-ethoxy-2,6-dimethyl-L-tyrosine

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With hydrogen iodide for 4h; Reagent/catalyst; Reflux;	91%

: 99953-00-1
(S)-N-Boc-2,6-dimethyltyrosine

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With hydrogenchloride In water	83%

: (2S)-2-amino-1-((6R,7aR)-8,8-dimethyl-2,2-dioxidotetrahydro-3H-3a,6-methanobenzo[c]isothiazol-1(4H)-yl)-3-(4-hydroxy-2,6-dimethylphenyl)propan-1-one

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With lithium hydroxide In tetrahydrofuran at 0℃; for 1h;	82%

: C34H32ClN3NiO4

A: 1616506-47-8
(R)-N-(2-benzoyl-4-chlorophenyl)-2-((1-phenylethyl)amino)acetamide

B: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With hydrogenchloride In methanol at 50℃; for 4h;	A n/a B 75.1%

: 126312-59-2
N-Acetyl-2,6 dimethyl-O-methyl-(S)-tyrosine methyl ester

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With hydrogen bromide Heating;

: 90609-47-5
1-iodo-2,6-dimethyl-4-methoxybenzene

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N / Pd(OAc)2, tri-o-tolylphosphine / acetonitrile / Heating 2: H2 / BF4 / ethyl acetate / 60 °C 3: 48percent HBr / Heating View Scheme

: 126312-58-1
Methyl-(Z)-α-acetamido-β-(2,6-dimethyl-4methoxyphenyl) acrylate

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: H2 / BF4 / ethyl acetate / 60 °C 2: 48percent HBr / Heating View Scheme

: 1255098-61-3
N-acetyl-2,6-dimethyl-DL-tyrosine

A: 1310488-05-1
(R)-N-acetyl-2,6-dimethyltyrosine

B: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With acylase I from porcine kidney; cobalt(II) chloride; sodium hydroxide at 40℃; for 24h; pH=8; aq. phosphate buffer; Enzymatic reaction; optical yield given as %ee; enantioselective reaction;

: 1333148-31-4
(S)-N-acetyl-2,6-dimethyltyrosine

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With hydrogenchloride; acylase I from porcine kidney at 35℃; for 72h; pH=8; Enzymatic reaction; enantioselective reaction;

: 80826-86-4
4-iodo-3,5-dimethylphenol

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1.1: pyridine / 10 °C 1.2: 39 - 55 °C / Large scale reaction 2.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine 3.1: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr 4.1: hydrogenchloride; water / 30 - 90 °C 4.2: 40 - 47 °C / pH 4 View Scheme
Multi-step reaction with 5 steps 1.1: pyridine / 10 °C 1.2: 39 - 55 °C / Large scale reaction 2.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine 3.1: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr 4.1: cobalt(II) chloride; sodium hydroxide / 35 °C / pH 8 - 10 / aq. phosphate buffer 5.1: hydrogenchloride; acylase I from porcine kidney / 72 h / 35 °C / pH 8 / Enzymatic reaction View Scheme

Yield

Multi-step reaction with 4 steps
1.1: pyridine / 10 °C
1.2: 39 - 55 °C / Large scale reaction
2.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine
3.1: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr
4.1: hydrogenchloride; water / 30 - 90 °C
4.2: 40 - 47 °C / pH 4
View Scheme

Multi-step reaction with 5 steps
1.1: pyridine / 10 °C
1.2: 39 - 55 °C / Large scale reaction
2.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine
3.1: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr
4.1: cobalt(II) chloride; sodium hydroxide / 35 °C / pH 8 - 10 / aq. phosphate buffer
5.1: hydrogenchloride; acylase I from porcine kidney / 72 h / 35 °C / pH 8 / Enzymatic reaction
View Scheme

: 145235-84-3
3,5-dimethyl-4-iodophenol acetate

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine 2.1: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr 3.1: hydrogenchloride; water / 30 - 90 °C 3.2: 40 - 47 °C / pH 4 View Scheme
Multi-step reaction with 4 steps 1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine 2: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr 3: cobalt(II) chloride; sodium hydroxide / 35 °C / pH 8 - 10 / aq. phosphate buffer 4: hydrogenchloride; acylase I from porcine kidney / 72 h / 35 °C / pH 8 / Enzymatic reaction View Scheme

: 145235-85-4
methyl (Z)-2-acetamido-3-(4-acetoxy-2,6-dimethylphenyl)-2-propenoate

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1.1: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr 2.1: hydrogenchloride; water / 30 - 90 °C 2.2: 40 - 47 °C / pH 4 View Scheme
Multi-step reaction with 3 steps 1: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr 2: cobalt(II) chloride; sodium hydroxide / 35 °C / pH 8 - 10 / aq. phosphate buffer 3: hydrogenchloride; acylase I from porcine kidney / 72 h / 35 °C / pH 8 / Enzymatic reaction View Scheme

: 145235-86-5
(S)-4-acetoxy-N-acetyl-2,6-dimethylphenylalanine methyl ester

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Stage #1: (S)-4-acetoxy-N-acetyl-2,6-dimethylphenylalanine methyl ester With hydrogenchloride; water at 30 - 90℃; Stage #2: With sodium hydroxide In water at 40 - 47℃; pH=4;
Multi-step reaction with 2 steps 1: cobalt(II) chloride; sodium hydroxide / 35 °C / pH 8 - 10 / aq. phosphate buffer 2: hydrogenchloride; acylase I from porcine kidney / 72 h / 35 °C / pH 8 / Enzymatic reaction View Scheme

: 108-68-9
3,5-Dimethylphenol

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1.1: hydrogenchloride; potassium iodate; potassium iodide / methanol; water / 0 - 20 °C / Large scale reaction 2.1: pyridine / 10 °C 2.2: 39 - 55 °C / Large scale reaction 3.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine 4.1: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr 5.1: hydrogenchloride; water / 30 - 90 °C 5.2: 40 - 47 °C / pH 4 View Scheme
Multi-step reaction with 6 steps 1.1: hydrogenchloride; potassium iodate; potassium iodide / methanol; water / 0 - 20 °C / Large scale reaction 2.1: pyridine / 10 °C 2.2: 39 - 55 °C / Large scale reaction 3.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine 4.1: [Rh(1,5-COD)(S,S-Et-FerroTANE)]BF4; hydrogen / ethyl acetate / 16 h / 60 °C / 3750.38 Torr 5.1: cobalt(II) chloride; sodium hydroxide / 35 °C / pH 8 - 10 / aq. phosphate buffer 6.1: hydrogenchloride; acylase I from porcine kidney / 72 h / 35 °C / pH 8 / Enzymatic reaction View Scheme
Multi-step reaction with 5 steps 1.1: triethylamine / dichloromethane / 1 h / 20 °C 2.1: zinc(II) chloride; chlorosulfonic acid / 0.5 h / -10 °C 2.2: 2 h / 5 - 10 °C 3.1: N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium / tetrahydrofuran / 0.17 h / -78 °C / Inert atmosphere 3.2: 3 h / -78 - 20 °C / Inert atmosphere 4.1: hydrogenchloride / tetrahydrofuran; water / 4 h / 0 °C 5.1: lithium hydroxide / tetrahydrofuran / 1 h / 0 °C View Scheme

: FMoc-L-2,6-dimethyltyrosine

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With piperidine In N,N-dimethyl-formamide at 20℃; for 2.33333h;	4.3 g

: 95741-44-9
1-((4-bromo-3,5-dimethylphenoxy)methyl)benzene

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1.1: magnesium / tetrahydrofuran / 6 h / 25 °C / Reflux 1.2: 25 °C 2.1: methanol / 5 h / 25 °C 3.1: sodium periodate / tetrachloromethane; acetonitrile; water / 5 h 4.1: palladium 10% on activated carbon; hydrogen / methanol / 24 h / 2068.65 Torr View Scheme

: (2R,3S)-1,2-isopropylidene-3-(tert-butoxycarbonyl)amino-4-[(4-benzyloxy-2,6-dimethyl)phenyl]butane-1,2-diol

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: methanol / 5 h / 25 °C 2: sodium periodate / tetrachloromethane; acetonitrile; water / 5 h 3: palladium 10% on activated carbon; hydrogen / methanol / 24 h / 2068.65 Torr View Scheme

: 945669-52-3
(S)-O-benzyl-N-(tert-butoxycarbonyl)-2,6-dimethyltyrosine

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
With palladium 10% on activated carbon; hydrogen In methanol under 2068.65 Torr; for 24h;

: 26177-58-2
3,5-Dimethylphenyl ethyl carbonate

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1.1: zinc(II) chloride; chlorosulfonic acid / 0.5 h / -10 °C 1.2: 2 h / 5 - 10 °C 2.1: N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium / tetrahydrofuran / 0.17 h / -78 °C / Inert atmosphere 2.2: 3 h / -78 - 20 °C / Inert atmosphere 3.1: hydrogenchloride / tetrahydrofuran; water / 4 h / 0 °C 4.1: lithium hydroxide / tetrahydrofuran / 1 h / 0 °C View Scheme

Yield

Multi-step reaction with 4 steps
1.1: zinc(II) chloride; chlorosulfonic acid / 0.5 h / -10 °C
1.2: 2 h / 5 - 10 °C
2.1: N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium / tetrahydrofuran / 0.17 h / -78 °C / Inert atmosphere
2.2: 3 h / -78 - 20 °C / Inert atmosphere
3.1: hydrogenchloride / tetrahydrofuran; water / 4 h / 0 °C
4.1: lithium hydroxide / tetrahydrofuran / 1 h / 0 °C
View Scheme

: 54373-50-1
O-ethoxycarbonyl-3,5-dimethyl-4-chloromethylphenol

: 123715-02-6
H-Dmt

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium / tetrahydrofuran / 0.17 h / -78 °C / Inert atmosphere 1.2: 3 h / -78 - 20 °C / Inert atmosphere 2.1: hydrogenchloride / tetrahydrofuran; water / 4 h / 0 °C 3.1: lithium hydroxide / tetrahydrofuran / 1 h / 0 °C View Scheme

: 501-53-1
benzyl chloroformate

: 123715-02-6
H-Dmt

: 137764-59-1
2,6-dimethyl-N-<(phenylmethoxy)carbonyl>-L-tyrosine

Conditions

Conditions	Yield
With sodium hydroxide for 16h;	70%
Stage #1: H-Dmt With sodium hydrogencarbonate In 1,4-dioxane; water for 0.166667h; Stage #2: benzyl chloroformate In 1,4-dioxane; water at 20℃; for 2h;	6 g

: 123715-02-6
H-Dmt

: 543-27-1
isobutyl chloroformate

: C16H23NO5

Conditions

Conditions	Yield
With 4-methyl-morpholine In tetrahydrofuran at -23℃; for 0.75h;

: 24424-99-5
di-tert-butyl dicarbonate

: 123715-02-6
H-Dmt

: 99953-00-1
(S)-N-Boc-2,6-dimethyltyrosine

Conditions

Conditions	Yield
With sodium hydroxide In tert-butyl alcohol at 0 - 20℃; for 27h;
With triethylamine
Stage #1: di-tert-butyl dicarbonate; H-Dmt With water; sodium hydroxide at 20℃; for 72h; pH=8 - 10; Stage #2: With hydrogenchloride In water; ethyl acetate for 0.166667h; pH=4;	689 g

: 67-56-1
methanol

: 123715-02-6
H-Dmt

: 928195-92-0
(S)-2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionic acid methyl ester

Conditions

Conditions	Yield
With thionyl chloride In methanol

: 925672-53-3
(2S,3S)-β-methylcyclohexylalanine

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 74163-81-8
L-Tic-OH

: 123715-02-6
H-Dmt

: 2-[2-({2-[2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionyl]-1,2,3,4-tetrahydro-isoquinoline-3-carbonyl}-amino)-3-cyclohexyl-butyrylamino]-3-phenyl-propionic acid

Conditions

Conditions	Yield
Multistep reaction;

...Expand

: 925672-53-3
(2S,3S)-β-methylcyclohexylalanine

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 74163-81-8
L-Tic-OH

: 123715-02-6
H-Dmt

: 2-[2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionyl]-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid [1-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-cyclohexyl-propyl]-amide

Conditions

Conditions	Yield
Multistep reaction;

...Expand

: (2R,3S)-β-methylcyclohexylalanine

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 74163-81-8
L-Tic-OH

: 123715-02-6
H-Dmt

: 2-[2-({2-[2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionyl]-1,2,3,4-tetrahydro-isoquinoline-3-carbonyl}-amino)-3-cyclohexyl-butyrylamino]-3-phenyl-propionic acid

Conditions

Conditions	Yield
Multistep reaction;

...Expand

: (2R,3S)-β-methylcyclohexylalanine

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 74163-81-8
L-Tic-OH

: 123715-02-6
H-Dmt

: 2-[2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionyl]-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid [1-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-cyclohexyl-propyl]-amide

Conditions

Conditions	Yield
Multistep reaction;

...Expand

: (2S,3R)-β-methylcyclohexylalanine

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 74163-81-8
L-Tic-OH

: 123715-02-6
H-Dmt

: 2-[2-({2-[2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionyl]-1,2,3,4-tetrahydro-isoquinoline-3-carbonyl}-amino)-3-cyclohexyl-butyrylamino]-3-phenyl-propionic acid

Conditions

Conditions	Yield
Multistep reaction;

...Expand

: (2S,3R)-β-methylcyclohexylalanine

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 74163-81-8
L-Tic-OH

: 123715-02-6
H-Dmt

: 2-[2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionyl]-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid [1-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-cyclohexyl-propyl]-amide

Conditions

Conditions	Yield
Multistep reaction;

...Expand

: 925672-54-4
(2R,3R)-β-methylcyclohexylalanine

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 74163-81-8
L-Tic-OH

: 123715-02-6
H-Dmt

: 2-[2-({2-[2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionyl]-1,2,3,4-tetrahydro-isoquinoline-3-carbonyl}-amino)-3-cyclohexyl-butyrylamino]-3-phenyl-propionic acid

Conditions

Conditions	Yield
Multistep reaction;

...Expand

: 925672-54-4
(2R,3R)-β-methylcyclohexylalanine

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 74163-81-8
L-Tic-OH

: 123715-02-6
H-Dmt

: 2-[2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionyl]-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid [1-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-cyclohexyl-propyl]-amide

Conditions

Conditions	Yield
Multistep reaction;

...Expand

: 67-56-1
methanol

: 123715-02-6
H-Dmt

: (S)-2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionic acid methyl ester; hydrochloride

Conditions

Conditions	Yield
Stage #1: H-Dmt With thionyl chloride Stage #2: methanol Further stages.;

: 123715-02-6
H-Dmt

: 331283-95-5
H-Dmt-NH2

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: SOCl2 / methanol 2: Et3N 3: NH3 / methanol 4: HCl / dioxane View Scheme

: 123715-02-6
H-Dmt

: 2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-N-methoxy-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N 2: HCl / dioxane View Scheme

: 123715-02-6
H-Dmt

: H-Dmt-NH-CH3

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N 2: HCl / dioxane View Scheme

: 123715-02-6
H-Dmt

: (S)-2-Dimethylamino-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: SOCl2 / methanol 2: Et3N 3: NH3 / methanol 4: HCl / dioxane 5: NaBH3CN / dioxane View Scheme

: 123715-02-6
H-Dmt

: 2-amino-N-hydroxy-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N 2: NH2OH 3: HCl / dioxane View Scheme

: 123715-02-6
H-Dmt

: 2-amino-N-ethyl-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N 2: HCl / dioxane View Scheme

: 123715-02-6
H-Dmt

: 2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-N-isopropyl-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N 2: HCl / dioxane View Scheme

: 123715-02-6
H-Dmt

: 2-amino-N-aminomethyl-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N 2: HCl / dioxane View Scheme

: 123715-02-6
H-Dmt

: 2-amino-N-tert-butyl-3-(4-hydroxy-2,6-dimethyl-phenyl)-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N 2: HCl / dioxane View Scheme

: 123715-02-6
H-Dmt

: 2-amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-N-propyl-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N 2: PyBOP; N,N-diisopropylethylamine 3: HCl / dioxane View Scheme

2,6-Dimethyl-L-tyrosine Specification

The CAS register number of 2,6-Dimethyl-L-tyrosine is 123715-02-6. It also can be called as L-Tyrosine,2,6-dimethyl- and the IUPAC name about this chemical is (2S)-2-amino-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid. The molecular formula about this chemical is C₁₁H₁₅NO₃and the molecular weight is 209.24. It belongs to the following product categories, such as Pharmacetical; Benzene series; API intermediates; Non-natural amino acids and so on.

Physical properties about 2,6-Dimethyl-L-tyrosine are: (1)ACD/LogP: 1.30; (2)ACD/LogD (pH 5.5): -1.2; (3)ACD/LogD (pH 7.4): -1.21; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 1; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 4; (9)#H bond donors: 4; (10)#Freely Rotating Bonds: 5; (11)Polar Surface Area: 38.77Å²; (12)Index of Refraction: 1.592; (13)Molar Refractivity: 57.02 cm³; (14)Molar Volume: 168.4 cm³; (15)Polarizability: 22.6x10^-24cm³; (16)Surface Tension: 56.7 dyne/cm; (17)Enthalpy of Vaporization: 70.16 kJ/mol; (18)Boiling Point: 412.8 °C at 760 mmHg; (19)Vapour Pressure: 1.49E-07 mmHg at 25°C.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C(O)[C@@H](N)Cc1c(cc(O)cc1C)C
(2)InChI: InChI=1/C11H15NO3/c1-6-3-8(13)4-7(2)9(6)5-10(12)11(14)15/h3-4,10,13H,5,12H2,1-2H3,(H,14,15)/t10-/m0/s1
(3)InChIKey: LSNDLIKCFHLFKO-JTQLQIEIBF
(4)Std. InChI: InChI=1S/C11H15NO3/c1-6-3-8(13)4-7(2)9(6)5-10(12)11(14)15/h3-4,10,13H,5,12H2,1-2H3,(H,14,15)/t10-/m0/s1
(5)Std. InChIKey: LSNDLIKCFHLFKO-JTQLQIEISA-N

Product Name

2,6-Dimethyl-L-tyrosine

Synthetic route

2,6-Dimethyl-L-tyrosine Specification

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