Br-C10-methyl ester

Names

[ Name ]:
Br-C10-methyl ester

[Synonym ]:
MFCD00045047
methyl 11-bromoundecan-1-oate
11-bromo-undecanoic acid methyl ester
11-Brom-undecansaeure-methylester
methyl 11-bromoundecanate
11-Brom-undecylsaeure-methylester

Biological Activity

[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].

[Related Catalog]:

Research Areas >> Cancer

Signaling Pathways >> PROTAC >> PROTAC Linker

[Target]

Alkyl/ether

[References]

[1]. Wei J, et al. Discovery of a First-in-Class Mitogen-Activated Protein Kinase Kinase 1/2 Degrader.J Med Chem. 2019 Dec 12;62(23):10897-10911.

Chemical & Physical Properties

[ Density]:
1.157 g/mL at 25ºC(lit.)

[ 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.)

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2915900090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2915900090

[ 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%

Articles

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...

Studies on ω-Oxidation of Fatty Acids in vitro. KAMEI S, et al.

J. Biochem. 56(1) , 72-76, (1964)

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)