Phenyl dihydrogen orthoborate

Base Information

• Chemical Name: Phenyl dihydrogen orthoborate
• CAS No.: 4688-74-8
• Molecular Formula: C6H7 B O3
• Molecular Weight: 137.931
• European Community (EC) Number: 225-145-9
• DSSTox Substance ID: DTXSID60196973
• Nikkaji Number: J139.229H
• Wikidata: Q83069948
• Mol file: 4688-74-8.mol

Synonyms:Phenyl dihydrogen orthoborate;4688-74-8;EINECS 225-145-9;C6H7BO3;phenyl boric acid;Borsaurephenylester;Boric acid phenyl ester;SCHEMBL78440;DTXSID60196973;C6-H7-B-O3

Chemical Property of Phenyl dihydrogen orthoborate

Chemical Property:

• Vapor Pressure: 0.00541mmHg at 25°C
• Boiling Point: 262.7°Cat760mmHg
• Flash Point: 112.7°C
• PSA: 49.69000
• Density: 1.211g/cm³
• LogP: 0.03490
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 138.0488242
• Heavy Atom Count: 10
• Complexity: 91

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: B(O)(O)OC1=CC=CC=C1

Technology Process of Phenyl dihydrogen orthoborate

There total 4 articles about Phenyl dihydrogen orthoborate 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:

bis(ethylamino)phenylborane (90976-49-1) → phenylboric acid (4688-74-8)

Guidance literature:

With water; byproducts: C2H5NH2; hydrolysis at room temp.;

Reference yield:

phenylborondichloride (873-51-8) → phenylboric acid (4688-74-8)

Guidance literature:

Multi-step reaction with 2 steps

2: water

With water;

Reference yield:

C6H5B(S-n-C4H9)N(C2H5)2 (92431-82-8) → phenylboric acid (4688-74-8)

Guidance literature:

Multi-step reaction with 2 steps

2: water

With water;

upstream raw materials:

bis(ethylamino)phenylborane

phenylborondichloride

C₆H₅B(S-n-C₄H₉)N(C₂H₅)2

Downstream raw materials:

methyl 2-phenoxybenzoate

10-methoxydibenzo[b,f][1,4]oxazepin-11(10H)-one

N-methoxy-2-phenoxybenzamide

4,7-diphenyl-2,1,3-benzothiadiazole

Refernces

• 1、 -. "Ligands for ADH: cinchona alkaloids and moderately sized organic substituents linked through a planar aromatic spacer group". . . Retrieved 2008/06/13.