Br-C10-methyl ester structure
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Common Name | Br-C10-methyl ester | ||
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CAS Number | 6287-90-7 | Molecular Weight | 279.21400 | |
Density | 1.157 g/mL at 25ºC(lit.) | Boiling Point | 115ºC0.04 mm Hg(lit.) | |
Molecular Formula | C12H23BrO2 | Melting Point | 13°C(lit.) | |
MSDS | USA | Flash Point | >230 °F |
Use of Br-C10-methyl esterBr-C10-methyl ester is a PROTAC linker, which refers to the alkyl/ether composition. Br-C10-methyl ester is used in the synthesis of a series of PROTACs (MS432). PROTACs contain two different ligands connected by a linker; one is the VHL ligand portion and the other is for the target protein[1]. |
Name | methyl 11-bromoundecanoate |
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Synonym | More Synonyms |
Description | Br-C10-methyl ester is a PROTAC linker, which refers to the alkyl/ether composition. Br-C10-methyl ester is used in the synthesis of a series of PROTACs (MS432). PROTACs contain two different ligands connected by a linker; one is the VHL ligand portion and the other is for the target protein[1]. |
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Related Catalog | |
Target |
Alkyl/ether |
References |
Density | 1.157 g/mL at 25ºC(lit.) |
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Boiling Point | 115ºC0.04 mm Hg(lit.) |
Melting Point | 13°C(lit.) |
Molecular Formula | C12H23BrO2 |
Molecular Weight | 279.21400 |
Flash Point | >230 °F |
Exact Mass | 278.08800 |
PSA | 26.30000 |
LogP | 4.06520 |
Index of Refraction | n20/D 1.465(lit.) |
Personal Protective Equipment | Eyeshields;Gloves |
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RIDADR | NONH for all modes of transport |
HS Code | 2915900090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2915900090 |
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Summary | 2915900090 other saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:5.5% General tariff:30.0% |
Versatile synthesis of phenoxydiazirine-based fatty acid analogues and photoreactive galactosylceramide.
Bioorg. Med. Chem. Lett. 12(1) , 89-91, (2002) A versatile synthesis of diazirine-based photoreactive fatty acid analogues is reported. The key step is phenoxy alkylation of diazirine with halo alkyl acid esters. The conditions described will be a... |
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Studies on ω-Oxidation of Fatty Acids in vitro. KAMEI S, et al.
J. Biochem. 56(1) , 72-76, (1964)
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A Three Step Synthesis of 11-Cycloheptylundecanoic Acid, a Component of the Thermoacidophile Alicyclobacillus cycloheptanicus. Hassarajani SA and Mamdapur VR.
Molecules 3(2) , 41-43, (1998)
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MFCD00045047 |
methyl 11-bromoundecan-1-oate |
11-bromo-undecanoic acid methyl ester |
11-Brom-undecansaeure-methylester |
methyl 11-bromoundecanate |
11-Brom-undecylsaeure-methylester |