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(4-Boc-Aminophenyl)Boronic Acid

Base Information Edit
  • Chemical Name:(4-Boc-Aminophenyl)Boronic Acid
  • CAS No.:380430-49-9
  • Molecular Formula:C11H16BNO4
  • Molecular Weight:237.063
  • Hs Code.:29319090
  • European Community (EC) Number:670-415-5
  • DSSTox Substance ID:DTXSID40394192
  • Nikkaji Number:J1.962.976G
  • Wikidata:Q72513926
  • Mol file:380430-49-9.mol
(4-Boc-Aminophenyl)Boronic Acid

Synonyms:380430-49-9;(4-Boc-Aminophenyl)Boronic Acid;4-BOC-aminophenylboronic acid;4-(N-Boc-amino)phenylboronic acid;(4-((tert-Butoxycarbonyl)amino)phenyl)boronic acid;4-(Boc-amino)phenylboronic Acid;[4-[(2-methylpropan-2-yl)oxycarbonylamino]phenyl]boronic Acid;4-(tert-Butoxycarbonylamino)phenylboronic acid;4-(BOC-AMINO)BENZENEBORONIC ACID;(4-{[(tert-butoxy)carbonyl]amino}phenyl)boronic acid;4-[(tert-butoxycarbonyl)amino]phenylboronic acid;MFCD02093054;{4-[(Tert-butoxycarbonyl)amino]phenyl}boronic acid;4-Aminobenzeneboronic acid, N-BOC protected;4-(tert-Butoxycarbonyl)aminophenylboronic acid;[4-(tert-butoxycarbonylamino)phenyl]boronic acid;SCHEMBL59499;(4-Boc-Aminophenyl)BoronicAcid;DTXSID40394192;UBVOLHQIEQVXGM-UHFFFAOYSA-N;BCP13306;STR09000;4-(N-Boc-amino)phenyl boronic acid;AKOS015841448;AB10732;CS-W000923;NCGC00249486-01;NCGC00249486-02;AC-22732;SY017933;4-tert-Butoxycarbonylaminophenylboronic acid;4(tert-butoxycarbonylamino)phenylboronic acid;4-(tertbutoxycarbonylamino)phenylboronic acid;4-tert-Butoxycarbonylamino-phenylboronic acid;AM20050346;B4335;FT-0602176;(4-tert-Butoxycarbonylaminophenyl)-boronic acid;4-(N-Boc-amino)phenylboronic acid, >=95.0%;4-(tert-butoxy carbonylamino)phenylboronic acid;4-(tert-butoxycarbonylamino) phenylboronic acid;4-(tert-butoxycarbonylamino)phenyl boronic acid;EN300-312230;4-(tert-butyloxycarbonylamino)phenylboronic acid;{4-[(tertbutoxycarbonyl)amino]phenyl}boronic acid;4-(T-BUTOXYCARBONYLAMINO)PHENYLBORONIC ACID;4-[(tert-butoxycarbonyl)amino]benzeneboronic acid;{4-[(tert-butoxycarbonyl) amino]phenyl}boronic acid;J-513863;{4-[(tert-butoxycarbonyl) amino]phenyl} boronic acid;Z1505697238;[4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)phenyl]boronic acid

Suppliers and Price of (4-Boc-Aminophenyl)Boronic Acid
Supply Marketing:Edit
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
  • 4-Boc-aminophenylboronicAcid
  • 100mg
  • $ 45.00
  • TCI Chemical
  • 4-[(tert-Butoxycarbonyl)amino]phenylboronic Acid (contains varying amounts of Anhydride)
  • 1g
  • $ 71.00
  • TCI Chemical
  • 4-[(tert-Butoxycarbonyl)amino]phenylboronic Acid (contains varying amounts of Anhydride)
  • 5g
  • $ 279.00
  • Synthonix
  • 4-(tert-Butoxycarbonyl)aminophenylboronicacid 95%
  • 100g
  • $ 730.00
  • Synthonix
  • 4-(tert-Butoxycarbonyl)aminophenylboronicacid 95%
  • 25g
  • $ 180.00
  • Synthonix
  • 4-(tert-Butoxycarbonyl)aminophenylboronicacid 95%
  • 10g
  • $ 100.00
  • Synthonix
  • 4-(tert-Butoxycarbonyl)aminophenylboronicacid 95%
  • 5g
  • $ 70.00
  • Synthonix
  • 4-(tert-Butoxycarbonyl)aminophenylboronicacid 95%
  • 1g
  • $ 20.00
  • SynQuest Laboratories
  • 4-Aminobenzeneboronic acid, N-Boc protected
  • 1 g
  • $ 21.00
  • SynQuest Laboratories
  • 4-Aminobenzeneboronic acid, N-Boc protected
  • 5 g
  • $ 87.00
Total 76 raw suppliers
Chemical Property of (4-Boc-Aminophenyl)Boronic Acid Edit
Chemical Property:
  • Appearance/Colour:White to light yellow crystal powder 
  • Melting Point:199-204 °C (dec.)(lit.) 
  • Refractive Index:1.53 
  • PKA:8?+-.0.17(Predicted) 
  • PSA:78.79000 
  • Density:1.18 g/cm3 
  • LogP:0.78640 
  • Storage Temp.:Keep Cold 
  • Solubility.:soluble in Methanol 
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:237.1172382
  • Heavy Atom Count:17
  • Complexity:257
Purity/Quality:

4-Boc-aminophenylboronicAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37/39-24/25 
MSDS Files:
Useful:
  • Canonical SMILES:B(C1=CC=C(C=C1)NC(=O)OC(C)(C)C)(O)O
  • Uses suzuki reaction Boronic acid used in a study of the rhodium-catalyzed desymmetrization of a meso-cyclic allylic dicarbonate via SN2′ substitution.
Technology Process of (4-Boc-Aminophenyl)Boronic Acid

There total 4 articles about (4-Boc-Aminophenyl)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:
Guidance literature:
With hydrogenchloride; polystyrene boronic acid; In acetonitrile; at 20 ℃; for 18h;
DOI:10.1016/j.tetlet.2004.07.014
Guidance literature:
With hydrogenchloride; water; In tetrahydrofuran; diethyl ether; hexane; at 0 ℃; for 0.25h;
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