2-Amino-2-methylpropanedioic acid

Base Information

Chemical Name:2-Amino-2-methylpropanedioic acid
CAS No.:26767-88-4
Molecular Formula:C4H7 N O4
Molecular Weight:133.104
Hs Code.:
DSSTox Substance ID:DTXSID301031069
Nikkaji Number:J20.698I
Mol file:26767-88-4.mol

Synonyms:2-amino-2-methylpropanedioic acid;26767-88-4;Amino(methyl)malonic acid;a-amino-a-methylmalonic acid;2-amino-2-methylmalonic acid;SCHEMBL1118781;DTXSID301031069;Propanedioic acid,aminomethyl-(9ci);AKOS006337796;CS-0527786

Suppliers and Price of 2-Amino-2-methylpropanedioic 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

Total 5 raw suppliers

Chemical Property of 2-Amino-2-methylpropanedioic acid

Chemical Property:

PSA：100.62000
LogP:-0.42670
XLogP3:-3.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:133.03750770
Heavy Atom Count:9
Complexity:139

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C(=O)O)(C(=O)O)N

Technology Process of 2-Amino-2-methylpropanedioic acid

There total 2 articles about 2-Amino-2-methylpropanedioic 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:

: 2-{[1-(3-Hydroxy-2-methyl-5-phosphonooxymethyl-pyridin-4-yl)-meth-(E)-ylidene]-amino}-2-methyl-malonic acid

: 26767-88-4
α-amino-α-methylmalonic acid

: 54-47-7
pyridoxal 5'-phosphate

Guidance literature:: With potassium chloride; potassium acetate; at 25 ℃; pH=5; Equilibrium constant;
DOI:10.1021/ja0026354

Reference yield:

: 133388-70-2
(3S,6S)-2,5-diethoxy-6-isopropyl-3-carboxymethyl-3-methyl-6-hydropyrazine

: 72-18-4,25609-85-2,7004-03-7,921-10-8
L-valine

: 26767-88-4
α-amino-α-methylmalonic acid

Guidance literature:: With hydrogenchloride; sodium hydroxide; Yield given. Multistep reaction; 1) CH₃CN, RT, 18h, 2) 70 deg C, 15 min;
DOI:10.1016/S0040-4020(01)90505-8

Reference yield:

: 26767-88-4
α-amino-α-methylmalonic acid

: 56-41-7,25191-17-7,18875-37-1
L-alanin

: 338-69-2,25191-17-7,18875-37-1
D-Alanine

Guidance literature:: With (6R,8R)-6,8-dimethyl-2,5,9,12-tetraazatridecanecobalt(III)Cl₂ ClO₄; Multistep reaction. Title compound not separated from byproducts;
DOI:10.1021/ja00399a075