Amino(3-methylphenyl)acetic acid

Base Information

Chemical Name:Amino(3-methylphenyl)acetic acid
CAS No.:53519-82-7
Molecular Formula:C₉H₁₁NO₂
Molecular Weight:165.192
Hs Code.:
European Community (EC) Number:865-387-8
DSSTox Substance ID:DTXSID40405636
Nikkaji Number:J1.289.637I
Mol file:53519-82-7.mol

Synonyms:2-amino-2-(3-methylphenyl)acetic Acid;amino(3-methylphenyl)acetic acid;53519-82-7;187979-43-7;AMino-(3-Methylphenyl)-acetic acid;2-amino-2-(m-tolyl)acetic acid;Amino-m-tolyl-acetic acid;SCHEMBL5293096;2-amino-2-(m-tolyl)aceticacid;DTXSID40405636;LUSUJXIQPCPYCT-UHFFFAOYSA-N;MFCD02662422;AKOS000178062;AKOS016051355;Dibenzo[c,f][2,7]naphthyridin-6-ol;AB32657;AB32661;BS-12240;BB 0249654;2-AMINO-2-(3-METHYLPHENYL)ACETICACID;EN300-75169;F78745;J-012105;BENZENEACETIC ACID, A-AMINO-3-METHYL-, (AR)-;Amino(3-methylphenyl)acetic acid (H-DL-Phg(3-Me)-OH);F2167-0080;Z317024596

Suppliers and Price of Amino(3-methylphenyl)acetic 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

TRC
2-Amino-2-(3-methylphenyl)aceticacid
50mg
$ 45.00

Activate Scientific
2-Amino-2-(3-methylphenyl)acetic acid 95+%
5 g
$ 584.00

Activate Scientific
2-Amino-2-(3-methylphenyl)acetic acid 95+%
1 g
$ 198.00

Acrotein
2-Amino-2-(3-methylphenyl)aceticacid 97%
1g
$ 146.67

Total 12 raw suppliers

Chemical Property of Amino(3-methylphenyl)acetic acid

Chemical Property:

XLogP3:-1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:165.078978594
Heavy Atom Count:12
Complexity:170

Purity/Quality:

98% Min ^*data from raw suppliers

2-Amino-2-(3-methylphenyl)aceticacid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=CC=C1)C(C(=O)O)N

Technology Process of Amino(3-methylphenyl)acetic acid

There total 9 articles about Amino(3-methylphenyl)acetic 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: 74.0%

: 271583-30-3
benzylamino-m-tolyl-acetic acid

: 53519-82-7
2-amino-2-(3-methylphenyl)acetic acid

Guidance literature:: With sodium hydroxide; hydrazine hydrate; palladium on activated charcoal; In water; for 10h; Heating;
DOI:10.1080/00397910008087127

Reference yield:

: 271583-72-3
N-benzyl amino-(3-methylphenyl)acetonitrile

: 53519-82-7
2-amino-2-(3-methylphenyl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / aq. H₂O₂; K₂CO₃ / dimethylsulfoxide / 16.5 h / 21 - 35 °C

2: 81 percent / NaOH; H₂O / various solvent(s) / 3.5 h / Heating

3: 74 percent / hydrazine hydrate; NaOH / Pd/C / H₂O; various solvent(s) / 10 h / Heating

With sodium hydroxide; water; dihydrogen peroxide; potassium carbonate; hydrazine hydrate; palladium on activated charcoal; In water; dimethyl sulfoxide; 1: Hydrolysis / 2: Hydrolysis / 3: Hydrogenolysis;
DOI:10.1080/00397910008087127

Reference yield:

: 620-23-5
m-tolyl aldehyde

: 53519-82-7
2-amino-2-(3-methylphenyl)acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: Na₂S₂O₅ / methanol; H₂O / 2 h / 35 °C

2: 94 percent / aq. H₂O₂; K₂CO₃ / dimethylsulfoxide / 16.5 h / 21 - 35 °C

3: 81 percent / NaOH; H₂O / various solvent(s) / 3.5 h / Heating

4: 74 percent / hydrazine hydrate; NaOH / Pd/C / H₂O; various solvent(s) / 10 h / Heating

With sodium metabisulfite; sodium hydroxide; water; dihydrogen peroxide; potassium carbonate; hydrazine hydrate; palladium on activated charcoal; In methanol; water; dimethyl sulfoxide; 1: Addition / 2: Hydrolysis / 3: Hydrolysis / 4: Hydrogenolysis;
DOI:10.1080/00397910008087127