(2R)-2-amino-3-(4-hydroxy-2-methylphenyl)propanoic acid

Base Information

Chemical Name:(2R)-2-amino-3-(4-hydroxy-2-methylphenyl)propanoic acid
CAS No.:128573-13-7
Molecular Formula:C₁₀H₁₃NO₃
Molecular Weight:195.218
Hs Code.:
DSSTox Substance ID:DTXSID50358664
Nikkaji Number:J1.417.221A
Mol file:128573-13-7.mol

Synonyms:128573-13-7;(2R)-2-amino-3-(4-hydroxy-2-methylphenyl)propanoic acid;2-METHYL-D-TYROSINE;AC1LIP71;SCHEMBL2903276;DTXSID50358664;N14843;(2R)-2-amino-3-(4-hydroxy-2-methylphenyl)propanoicacid

Suppliers and Price of (2R)-2-amino-3-(4-hydroxy-2-methylphenyl)propanoic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
(2R)-2-AMINO-3-(4-HYDROXY-2-METHYLPHENYL)PROPANOIC ACID 95.00%
5MG
$ 501.16

Acrotein
2-Methyl-D-tyrosine 97%
1g
$ 550.00

Total 1 raw suppliers

Chemical Property of (2R)-2-amino-3-(4-hydroxy-2-methylphenyl)propanoic acid

Chemical Property:

XLogP3:-1.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:195.08954328
Heavy Atom Count:14
Complexity:208

Purity/Quality:: (2R)-2-AMINO-3-(4-HYDROXY-2-METHYLPHENYL)PROPANOIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C=CC(=C1)O)CC(C(=O)O)N
Isomeric SMILES:CC1=C(C=CC(=C1)O)C[C@H](C(=O)O)N

Technology Process of (2R)-2-amino-3-(4-hydroxy-2-methylphenyl)propanoic acid

There total 10 articles about (2R)-2-amino-3-(4-hydroxy-2-methylphenyl)propanoic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 35186-98-2
7-hydroxy-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid

: 70680-92-1,128573-13-7,2370-56-1
2-methyl-L-tyrosine

: 128573-13-7,2370-56-1
D-2'-methyltyrosine

Guidance literature:: With hydrogen; palladium on activated charcoal; In acetic acid; at 60 ℃; for 24h; under 3800 Torr;
DOI:10.1016/S0223-5234(00)01171-5

Reference yield:

: 35186-98-2
7-hydroxy-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid

: 70680-92-1,128573-13-7,2370-56-1
2-methyl-L-tyrosine

: 128573-13-7,2370-56-1
D-2'-methyltyrosine

Guidance literature:: With hydrogen; palladium on activated charcoal; In acetic acid; at 60 ℃; for 24h; under 3800 Torr;
DOI:10.1016/S0223-5234(00)01171-5

Reference yield:

: 128-08-5
N-Bromosuccinimide

: diethyl acetimidomalonate

: 4685-47-6
3,4-dimethylanisole

: 96646-27-4,128573-13-7,2370-56-1
DL-2-methyl-p-tyrosine

Guidance literature:: With NaH; In tetrachloromethane; dimethylformanide; aqueous HBr; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide;