(4-(tert-Butylcarbamoyl)phenyl)boronic acid

Base Information

• Chemical Name: (4-(tert-Butylcarbamoyl)phenyl)boronic acid
• CAS No.: 850568-14-8
• Molecular Formula: C₁₁H₁₆BNO₃
• Molecular Weight: 221.064
• Hs Code.: 2931900090
• DSSTox Substance ID: DTXSID50378362
• Wikidata: Q82167890
• Mol file: 850568-14-8.mol

Synonyms:850568-14-8;(4-(tert-Butylcarbamoyl)phenyl)boronic acid;4-(tert-Butylaminocarbonyl)phenylboronic acid;[4-(tert-butylcarbamoyl)phenyl]boronic Acid;4-(tert-butylcarbamoyl)phenylboronic acid;4-(tert-Butylaminocarbonyl)benzeneboronic acid;N-T-BUTYL 4-BORONOBENZAMIDE;(4-(tert-Butylcarbamoyl)phenyl)boronicacid;SCHEMBL1961940;DTXSID50378362;JAIIZPWLCVMPFA-UHFFFAOYSA-N;MFCD03788413;AKOS015838076;AB15985;PS-9541;CS-0154874;[4-(tert-butylaminocarbonyl)phenyl]boronic acid;D71315;A853705;4-(tert-Butylaminocarbonyl)phenylboronic acid, AldrichCPR;[4-[[(1,1-Dimethylethyl)amino]carbonyl]phenyl]boronic acid

Chemical Property of (4-(tert-Butylcarbamoyl)phenyl)boronic acid

Chemical Property:

• Melting Point: 230-246 °C
• Refractive Index: 1.532
• PSA: 69.56000
• Density: 1.13 g/cm³
• LogP: 0.28560
• Storage Temp.: Keep Cold
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 221.1223235
• Heavy Atom Count: 16
• Complexity: 242

Purity/Quality:

97% ^*data from raw suppliers

4-(tert-Butylaminocarbonyl)benzeneboronic acid 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38-36
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of (4-(tert-Butylcarbamoyl)phenyl)boronic acid

There total 1 articles about (4-(tert-Butylcarbamoyl)phenyl)boronic 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: 70.7%

4-carboxyphenylboronic acid (14047-29-1) + tert-butylamine (75-64-9) → 4-(tert-butylcarbamoyl)phenylboronic acid (850568-14-8)

Guidance literature:

With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 0 - 25 ℃; for 6h;

upstream raw materials:

4-carboxyphenylboronic acid

tert-butylamine