Thiazoles
Organic heterocyclic compounds that consist of an azole with both sulfur and nitrogen atoms; includes compounds that are derived from thiazoles.
Quantity
- (2)
- (272)
- (25)
- (1)
- (2)
- (16)
- (3)
- (20)
- (6)
- (7)
- (68)
- (3)
- (2)
- (3)
- (80)
- (178)
- (2)
- (1)
- (5)
- (3)
- (1)
- (6)
Molecular Weight (g/mol)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (5)
- (4)
- (7)
- (3)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (1)
- (1)
- (3)
- (4)
- (2)
- (6)
- (1)
- (3)
- (1)
- (1)
- (4)
- (5)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (4)
- (13)
- (3)
- (3)
- (2)
- (2)
- (4)
- (6)
- (2)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (4)
- (1)
- (1)
- (4)
- (6)
- (1)
- (4)
- (8)
- (2)
- (3)
- (1)
- (1)
- (1)
- (3)
- (1)
- (3)
- (7)
- (1)
- (1)
- (1)
- (2)
- (1)
- (9)
- (1)
- (4)
- (1)
- (4)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (6)
- (5)
- (4)
- (1)
- (2)
- (6)
- (2)
- (2)
- (1)
- (6)
- (1)
- (2)
- (1)
- (5)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (3)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (4)
- (1)
- (2)
- (1)
- (2)
- (2)
- (3)
- (1)
- (2)
- (1)
- (5)
- (7)
- (1)
- (1)
- (3)
- (2)
- (4)
- (6)
- (5)
- (1)
- (1)
- (4)
- (2)
- (3)
- (2)
- (4)
- (2)
- (1)
- (3)
- (3)
- (3)
- (2)
- (2)
- (1)
- (2)
- (3)
- (4)
- (2)
- (3)
- (2)
- (1)
- (7)
- (3)
- (1)
- (5)
- (2)
- (3)
- (8)
- (1)
- (1)
- (2)
- (3)
- (2)
- (2)
- (4)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (4)
- (3)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (9)
- (2)
- (1)
- (2)
- (1)
- (2)
- (1)
- (3)
- (2)
- (1)
- (2)
- (1)
- (4)
- (3)
- (1)
- (4)
- (3)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (6)
- (1)
- (1)
- (1)
- (1)
- (1)
- (6)
- (1)
- (3)
- (2)
- (2)
- (4)
- (2)
- (2)
- (3)
- (3)
- (6)
- (2)
- (2)
- (1)
- (1)
- (3)
- (1)
- (2)
- (2)
- (2)
- (2)
- (3)
- (2)
- (1)
- (5)
- (1)
- (2)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (4)
- (2)
- (1)
- (2)
- (2)
- (2)
- (6)
- (1)
- (2)
- (2)
- (1)
- (4)
- (1)
- (3)
- (1)
- (20)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
Percent Purity
- (2)
- (1)
- (6)
- (2)
- (3)
- (1)
- (1)
- (2)
- (1)
- (8)
- (7)
- (2)
- (8)
- (1)
- (14)
- (43)
- (30)
- (1)
- (8)
- (23)
- (4)
- (1)
- (4)
- (2)
- (6)
- (2)
- (3)
- (14)
- (1)
- (1)
- (48)
- (10)
- (269)
- (69)
- (1)
- (12)
- (9)
Physical Form
- (3)
- (138)
- (2)
- (10)
- (1)
- (2)
- (33)
- (16)
- (29)
Boiling Point
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (3)
- (4)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (3)
- (3)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (4)
- (3)
- (2)
- (2)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (2)
- (3)
- (2)
- (1)
- (1)
- (1)
- (3)
- (2)
- (2)
- (1)
- (1)
- (1)
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796
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796
Aobchem AOBCHEM
5001007018 2 4-DIBROMO-6-PHENOXYANILINE 1
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797
Aobchem AOBCHEM
5001007027 2- 4-BROMO-3 5-DIFLUOROPHENYL
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798
Aobchem AOBCHEM
5001007083 3-BROMO-2 6-DIFLUOROPHENYL P
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799
Aobchem AOBCHEM
5001007405 2- 4-BROMO-2 3-DIFLUOROPHENYL
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800
Aobchem AOBCHEM
5001007579 METHYL 4- 2 6-DIFLUOROPHENYL
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801
Aobchem AOBCHEM
5001007580 METHYL 4- 2 6-DIFLUOROPHENYL
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802
Aobchem AOBCHEM
5001007790 3 5-DIBROMO-4-CHLOROPHENYL BO
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803
Aobchem AOBCHEM
5001007971 1- 3-BROMO-2 6-DIFLUOROPHENYL
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804
Aobchem AOBCHEM
5001007995 1- 3-BROMO-2 6-DIFLUOROPHENYL
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805
Aobchem AOBCHEM
5001008038 3 4-DIFLUOROPHENYL PROPYL SU
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806
Aobchem AOBCHEM
5001047302 2- O-TOLYL PYRIDINE 250MG
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807
Aobchem AOBCHEM
5001048222 N- 2 4-DIFLUOROPHENYL -2 2-DIM
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808
Medchemexpress LLC α-Methyltyrosine methyl ester hydrochloride | 7361-31-1 | MFCD00012606 | 98.9% | 245.71 | 5 G
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and Specialty Supplier Partner
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α-Methyltyrosine methyl ester hydrochloride is an orally active and competitive tyrosine hydroxylase inhibitor. It can inhibit the conversion of tyrosine to dopamine. It causes kidney damage and urethral calculi in rats and can be used as a tool for sympathetic nervous system research.
- Orally active
- Competitive tyrosine hydroxylase inhibitor
- Inhibits the conversion of tyrosine to dopamine
- Can be used as a tool for sympathetic nervous system research
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809
eMolecules 89711-08-0 | t-Butyl N-(2-oxoethyl)cabamate | Ochem Incorporation | MFCD01321273 | 159.185 | C7H13NO3 | 95.000 | CC(C)(C)OC(=O)NCC=O | 5g | 772471658
t-Butyl N-(2-oxoethyl)cabamate | Ochem Incorporation | 89711-08-0 | MFCD01321273 | 159.185 | C7H13NO3 | 95.000 | CC(C)(C)OC(=O)NCC=O | 5g | 772471658
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810
eMolecules 61074-71-3 | Ambeed | 3-Bromo-5-chloro-2-methylthiophene | 1g | 599118107 | A1452997 | MFCD19687381 | 211.5 | C5H4BrClS
Ambeed | 3-Bromo-5-chloro-2-methylthiophene | 1g | 599118107 | A1452997 | 61074-71-3 | MFCD19687381 | 211.500 | C5H4BrClS
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