(±)-2,2-Difluoro-1-methylcyclopropanecarboxylic+acid
Supplier:
AOB CHEM USA
Description:
4-Amino-3-fluorophenylboronic acid pinacol ester ≥97%
Catalog Number:
(76873-730)
Supplier:
AMBEED, INC
Description:
3-Amino-4-fluorophenylboronic acid pinacol ester 97%
Catalog Number:
(TS46597-2500)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Gemifloxacin mesylate
Catalog Number:
(100285-378)
Supplier:
Indofine Chemical Company
Description:
Fluoro Organics 351-35-9 25gm 204.15 Room temperature. 97%.
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Supplier:
BeanTown Chemical
Description:
CAS: 445-29-4; EC No: 207-158-1; MDL No: MFCD00002405; RTECS: DH0250000
Powder; Molecular Formula: C7H5FO2; MW: 140.11
Melting Point: 122-125°
Supplier:
Enzo Life Sciences
Description:
Potent MMP-13 inhibitor.
Supplier:
Adipogen
Description:
Fluorescent probe for thiols widely used in pre-column labeling of biological thiols for HPLC.
Supplier:
AOB CHEM USA
Description:
4-Amino-2-fluorophenylboronic acid pinacol ester ≥97%
Supplier:
AMBEED, INC
Description:
4-Fluorophenylboronic acid pinacol ester 97%
Supplier:
MP Biomedicals
Description:
5-Fluorodeoxyuridine is an antineoplastic agent, which acts as an antimetabolite. When administrated by rapid injection it acts as flurouracil, but when infused slowly, usually intra-arterially, it is converted to active F-dUMP, which leads to enhanced inhibition of DNA synthesis. It inhibits DNA synthesis by blocking thymidylic acid synthetase.
Supplier:
Matrix Scientific
Description:
MF=C11H15FN2O2 MW=226.25 CAS=579474-47-8 MDL=MFCD09701246 5G
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-Amino-2-fluorophenylboronic acid pinacol ester 97%
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
5-Methoxyisatin 97%
Supplier:
AMBEED, INC
Description:
(3-(Ethoxycarbonyl)-2-fluorophenyl)boronic acid, Purity: 97%, CAS Number: 1072952-52-3, Appearance: Solid, Storage: Inert atmosphere, Room Temperature, Size: 5G
Supplier:
AMBEED, INC
Description:
5-Methoxybenzoxazole-2-thiol 95%
Supplier:
Adipogen
Description:
Herbicide. Mode of action is similar to herbicides that inhibit the protoporphyrinogen oxidase (Protox) enzyme in susceptible plant species that leads to an uncontrolled nonenzymatic oxidation of protoporphyrinogen IX (Protogen) to protoporphyrin IX (Proto) and successive necrosis.
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