(Tert-butylamino)(phenyl)acetic acid

Base Information

Chemical Name:(Tert-butylamino)(phenyl)acetic acid
CAS No.:5466-04-6
Molecular Formula:C₁₂H₁₇NO₂
Molecular Weight:207.272
Hs Code.:
NSC Number:25991
DSSTox Substance ID:DTXSID10282456

Synonyms:5466-04-6;(tert-butylamino)(phenyl)acetic acid;NSC25991;2-(tert-butylamino)-2-phenylacetic acid;SCHEMBL6638248;DTXSID10282456;NSC-25991

Suppliers and Price of (Tert-butylamino)(phenyl)acetic acid

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of (Tert-butylamino)(phenyl)acetic acid

Chemical Property:

Vapor Pressure:0.000285mmHg at 25°C
Boiling Point:308.9°Cat760mmHg
Flash Point:140.6°C
Density:1.076g/cm³
XLogP3:-0.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:207.125928785
Heavy Atom Count:15
Complexity:214

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)NC(C1=CC=CC=C1)C(=O)O

Technology Process of (Tert-butylamino)(phenyl)acetic acid

There total 5 articles about (Tert-butylamino)(phenyl)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:

: 101-97-3
Ethyl 2-phenylethanoate

: 5466-04-6
N-Isobutyryl-C-phenylglycin

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / N-bromosuccinimide, benzoyl peroxide / CCl₄ / 6 h / Heating

2: 81 percent / tetrahydrofuran / 13 h / Heating

3: 10percent aq. NaOH / 1.17 h / Heating

With sodium hydroxide; N-Bromosuccinimide; Perbenzoic acid; In tetrahydrofuran; tetrachloromethane;
DOI:10.1002/jhet.5570330333

Reference yield:

: 2882-19-1,2216-90-2
ethyl 2-phenyl-2-bromoacetate

: 5466-04-6
N-Isobutyryl-C-phenylglycin

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / tetrahydrofuran / 13 h / Heating

2: 10percent aq. NaOH / 1.17 h / Heating

With sodium hydroxide; In tetrahydrofuran;
DOI:10.1002/jhet.5570330333