3-Bromo-alpha-methyl-4-(2-thiazolyl)benzeneacetic acid

Base Information

Chemical Name:3-Bromo-alpha-methyl-4-(2-thiazolyl)benzeneacetic acid
CAS No.:138568-62-4
Molecular Formula:C12H10BrNO2S
Molecular Weight:312.18200
Hs Code.:
DSSTox Substance ID:DTXSID70874275
Nikkaji Number:J425.239J
Mol file:138568-62-4.mol

Synonyms:138568-62-4;2-[3-bromo-4-(1,3-thiazol-2-yl)phenyl]propanoic acid;3-Bromo-alpha-methyl-4-(2-thiazolyl)benzeneacetic acid;DTXSID70874275;BENZENEACETIC ACID, 3-BROMO-?-METHYL-4-(2-THIAZO

Suppliers and Price of 3-Bromo-alpha-methyl-4-(2-thiazolyl)benzeneacetic 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 2 raw suppliers

Chemical Property of 3-Bromo-alpha-methyl-4-(2-thiazolyl)benzeneacetic acid

Chemical Property:

PSA：78.43000
LogP:3.76070
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:310.96156
Heavy Atom Count:17
Complexity:290

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C1=CC(=C(C=C1)C2=NC=CS2)Br)C(=O)O

Technology Process of 3-Bromo-alpha-methyl-4-(2-thiazolyl)benzeneacetic acid

There total 6 articles about 3-Bromo-alpha-methyl-4-(2-thiazolyl)benzeneacetic 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: 71.0%

: 138568-95-3
2-(3-Bromo-4-thiazol-2-yl-phenyl)-2-methyl-malonic acid diethyl ester

: 138568-62-4
2-<3-Bromo-4-(thiazol-2-yl)phenyl>propionic Acid

Guidance literature:: With potassium hydroxide; In ethanol; Heating;
DOI:10.1248/cpb.39.2323

Reference yield:

: 63860-31-1
2-bromo-4-chloro-1-nitrobenzene

: 138568-62-4
2-<3-Bromo-4-(thiazol-2-yl)phenyl>propionic Acid

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) NaH / 1.) DMF, 30 min, room temperature, 2.) DMF

2: H₂ / 10percent Pd-C / ethyl acetate / Ambient temperature

3: 1.) 12 N HCl, NaNO₂, 2.) Na₂CO₃ / 1.) H₂O, 2.) H₂O

4: 86 percent / H₂S (g), NEt₃ / dimethylformamide / 90 °C

5: 80 percent / HOAc, p-TsOH / 100 °C

6: 71 percent / KOH / ethanol / Heating

With hydrogenchloride; potassium hydroxide; hydrogen sulfide; hydrogen; sodium hydride; sodium carbonate; toluene-4-sulfonic acid; acetic acid; triethylamine; sodium nitrite; palladium on activated charcoal; In ethanol; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1248/cpb.39.2323

Reference yield:

: 138568-92-0
2-(3-Bromo-4-nitro-phenyl)-2-methyl-malonic acid diethyl ester

: 138568-62-4
2-<3-Bromo-4-(thiazol-2-yl)phenyl>propionic Acid

Guidance literature:: Multi-step reaction with 5 steps

1: H₂ / 10percent Pd-C / ethyl acetate / Ambient temperature

2: 1.) 12 N HCl, NaNO₂, 2.) Na₂CO₃ / 1.) H₂O, 2.) H₂O

3: 86 percent / H₂S (g), NEt₃ / dimethylformamide / 90 °C

4: 80 percent / HOAc, p-TsOH / 100 °C

5: 71 percent / KOH / ethanol / Heating

With hydrogenchloride; potassium hydroxide; hydrogen sulfide; hydrogen; sodium carbonate; toluene-4-sulfonic acid; acetic acid; triethylamine; sodium nitrite; palladium on activated charcoal; In ethanol; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1248/cpb.39.2323