4-Bromo-2-tert-butylbenzoic acid

Base Information

Chemical Name:4-Bromo-2-tert-butylbenzoic acid
CAS No.:14034-99-2
Molecular Formula:C₁₁H₁₃BrO₂
Molecular Weight:257.127
Hs Code.:
DSSTox Substance ID:DTXSID601272068
Mol file:14034-99-2.mol

Synonyms:4-bromo-2-tert-butylbenzoic acid;14034-99-2;4-bromo-2-(tert-butyl)benzoic acid;SCHEMBL898260;DTXSID601272068;4-bromo-2-(tert-butyl)benzoicacid;4-Bromo-2-(1,1-dimethylethyl)benzoic acid;CS-0224517;F73510;EN300-1198086

Suppliers and Price of 4-Bromo-2-tert-butylbenzoic acid

Supply Marketing:

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

Total 3 raw suppliers

Chemical Property of 4-Bromo-2-tert-butylbenzoic acid

Chemical Property:

PSA：37.30000
LogP:3.44480
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:256.00989
Heavy Atom Count:14
Complexity:220

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 4-Bromo-2-tert-butylbenzoic acid

There total 5 articles about 4-Bromo-2-tert-butylbenzoic 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:

: 59255-98-0
2-(tert-butyl)-4-nitroaniline

: 14034-99-2
4-Bromo-2-tert-butylbenzoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: (i) NaNO₂, aq. H₂SO₄, AcOH, (ii) /BRN= 4652394/, aq. CuCN

2: (i) aq. H₂SO₄, (ii) aq. NaNO₂, AcOH

3: H₂ / Raney-Ni / ethanol

4: (i) NaNO₂, aq. HBr, (ii) CuBr, aq. KBr

With hydrogen; nickel; In ethanol;

Reference yield:

: 14034-96-9
2-tert-butyl-4-nitrobenzonitrile

: 14034-99-2
4-Bromo-2-tert-butylbenzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: (i) aq. H₂SO₄, (ii) aq. NaNO₂, AcOH

2: H₂ / Raney-Ni / ethanol

3: (i) NaNO₂, aq. HBr, (ii) CuBr, aq. KBr

With hydrogen; nickel; In ethanol;

Reference yield:

: 14034-97-0
4-Nitro-2-tert.-butyl-benzoesaeure

: 14034-99-2
4-Bromo-2-tert-butylbenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Raney-Ni / ethanol

2: (i) NaNO₂, aq. HBr, (ii) CuBr, aq. KBr

With hydrogen; nickel; In ethanol;