2-(4-Biphenylyl)-2-(Boc-amino)acetic Acid

Base Information

• Chemical Name: 2-(4-Biphenylyl)-2-(Boc-amino)acetic Acid
• CAS No.: 946598-40-9
• Molecular Formula: C₁₁H₁₂FNO₃
• Molecular Weight: 225.22
• DSSTox Substance ID: DTXSID40596139
• Mol file: 946598-40-9.mol

Synonyms:369403-44-1;2-(4-Biphenylyl)-2-(Boc-amino)acetic Acid;2-([1,1'-Biphenyl]-4-yl)-2-((tert-butoxycarbonyl)amino)acetic acid;2-{[(tert-butoxy)carbonyl]amino}-2-(4-phenylphenyl)acetic acid;2-{[1,1'-biphenyl]-4-yl}-2-{[(tert-butoxy)carbonyl]amino}acetic acid;SCHEMBL3759870;DTXSID40596139;IGQRMCQSKDTFDV-UHFFFAOYSA-N;AC6017;MFCD02683167;a-(Boc-amino)-biphenyl-4-acetic acid;AKOS022184122;AB33250;AB33253;SY016273;DB-364020;CS-0214880;EN300-2008571;A874246;Z1200998440;2-(biphenyl-4-yl)-2-(tert-butoxycarbonylamino)acetic acid;([1,1'-Biphenyl]-4-yl)[(tert-butoxycarbonyl)amino]acetic acid;2-[(tert-butoxy)carbonylamino]-2-(4-phenylphenyl)acetic acid;2-([1,1'-Biphenyl]-4-yl)-2-((tert-butoxycarbonyl)amino)aceticacid;(2R)-2-[(TERT-BUTOXY)CARBONYLAMINO]-2-(4-PHENYLPHENYL)ACETIC ACID;(2S)-2-[(TERT-BUTOXY)CARBONYLAMINO]-2-(4-PHENYLPHENYL)ACETIC ACID;2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-(4-phenylphenyl)acetic acid

Chemical Property of 2-(4-Biphenylyl)-2-(Boc-amino)acetic Acid

Chemical Property:

• PSA: 49.77000
• LogP: 1.42550
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 327.14705815
• Heavy Atom Count: 24
• Complexity: 429

Purity/Quality:

97% ^*data from raw suppliers

2-Fluoro-4-morpholinobenzoicacid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)OC(=O)NC(C1=CC=C(C=C1)C2=CC=CC=C2)C(=O)O

Technology Process of 2-(4-Biphenylyl)-2-(Boc-amino)acetic Acid

There total 1 articles about 2-(4-Biphenylyl)-2-(Boc-amino)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:

C4H10BNO3 (1056475-77-4) + 2-fluoro-4-bromobenzoic acid (112704-79-7) → 2-fluoro-4-morpholinobenzoic acid (946598-40-9)

Guidance literature:

With potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tricyclohexylphosphine; In 1,4-dioxane; at 100 ℃; for 1h; Microwave irradiation;

DOI:10.1021/jm401067s

upstream raw materials:

C₄H₁₀BNO₃

2-fluoro-4-bromobenzoic acid