alpha-Methyl-4-(5-methyl-2-thiazolyl)benzeneacetic acid

Base Information

Chemical Name:alpha-Methyl-4-(5-methyl-2-thiazolyl)benzeneacetic acid
CAS No.:132483-43-3
Molecular Formula:C13H13NO2S
Molecular Weight:247.318
Hs Code.:
DSSTox Substance ID:DTXSID50874410
Nikkaji Number:J425.247K
Mol file:132483-43-3.mol

Synonyms:132483-43-3;alpha-Methyl-4-(5-methyl-2-thiazolyl)benzeneacetic acid;2-[4-(5-methyl-1,3-thiazol-2-yl)phenyl]propanoic acid;DTXSID50874410;BENZENEACETIC ACID, ?-METHYL-4-(5-METHYL-2-THIAZ

Suppliers and Price of alpha-Methyl-4-(5-methyl-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
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price

Total 1 raw suppliers

Chemical Property of alpha-Methyl-4-(5-methyl-2-thiazolyl)benzeneacetic acid

Chemical Property:

Boiling Point:422.2±47.0 °C(Predicted)
PKA:4.10±0.10(Predicted)
Density:1.246±0.06 g/cm3(Predicted)
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:247.06669983
Heavy Atom Count:17
Complexity:277

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CN=C(S1)C2=CC=C(C=C2)C(C)C(=O)O

Technology Process of alpha-Methyl-4-(5-methyl-2-thiazolyl)benzeneacetic acid

There total 6 articles about alpha-Methyl-4-(5-methyl-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:

: 100-00-5
4-chlorobenzonitrile

: 132483-43-3
2-[4-(5-Methyl-thiazol-2-yl)-phenyl]-propionic acid

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) NaH / 1.) DMF, 30 min, room temperature, 2.a) DMF, 30 min, room temperature, b.) 2 h, 90 deg C

2: 9.2 g / H₂ / 10percent Pd-C / ethyl acetate / 4 h / Ambient temperature

3: 1.) 12 N HCl, NaNO₂, 2.) Na₂CO₃ / 1.) H₂O, 2-3 deg C, 20 min, 2.a) H₂O, 1.5 h, 3 deg C, b.) 2 h, 50 deg C

4: 93 percent / H₂S (g), NEt₃ / dimethylformamide / 0.5 h / 90 °C

5: HOAc, p-TsOH / ethanol

6: 1 N aq. NaOH / ethanol / Heating

With hydrogenchloride; sodium 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:

: 61881-49-0
Diethyl 2-methyl-2-(4-nitrophenyl)malonate

: 132483-43-3
2-[4-(5-Methyl-thiazol-2-yl)-phenyl]-propionic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 9.2 g / H₂ / 10percent Pd-C / ethyl acetate / 4 h / Ambient temperature

2: 1.) 12 N HCl, NaNO₂, 2.) Na₂CO₃ / 1.) H₂O, 2-3 deg C, 20 min, 2.a) H₂O, 1.5 h, 3 deg C, b.) 2 h, 50 deg C

3: 93 percent / H₂S (g), NEt₃ / dimethylformamide / 0.5 h / 90 °C

4: HOAc, p-TsOH / ethanol

5: 1 N aq. NaOH / ethanol / Heating

With hydrogenchloride; sodium 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