909010-86-2

Basic information

• Product Name: 2-Thiophenecarboxylic acid, 5-broMo-3-Methyl-, ethyl ester
• Synonyms: 2-Thiophenecarboxylic acid, 5-broMo-3-Methyl-, ethyl ester
• CAS NO: 909010-86-2
• Molecular Formula: C8H9BrO2S
• Molecular Weight: 249.12486
• Mol File: 909010-86-2.mol

Chemical Properties

• Boiling Point: 277.8±35.0 °C(Predicted)
• Appearance: /
• Density: 1.502±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Thiophenecarboxylic acid, 5-broMo-3-Methyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Thiophenecarboxylic acid, 5-broMo-3-Methyl-, ethyl ester(909010-86-2)
• EPA Substance Registry System: 2-Thiophenecarboxylic acid, 5-broMo-3-Methyl-, ethyl ester(909010-86-2)

Safety Data

• Hazardous Substances Data: 909010-86-2(Hazardous Substances Data)

Upstream product

• 38239-45-1 5-bromo-3-methyl-thiophene-2-carboxylic acid 
• 64-17-5 ethanol 
• 14300-64-2 ethyl 3-methyl-2-thiophenecarboxylate 

Relevant articles and documents

ORGANIC COMPOUNDS

The present invention provides heterocyclic derivatives that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed.

2-SUBSTITUTED 5-MEMBERED HETEROCYCLES AS SCD INHIBITORS

The present invention provides heterocyclic derivatives that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed

Novel thienopyridine compounds, and methods of use thereof

The present invention relates to novel compounds capable of modulating the stability and/or activity of hypoxia inducible factor (HIF).

Convergent processes for the synthesis of a GARFT inhibitor containing a methyl substituted thiophene core and intermediates therefor

The invention relates to processes for the preparation of a GARFT inhibitor containing a methyl substituted thiophene core having the following structure: wherein each of R1 and R2 are independently a hydrogen atom or a moiety that together with the attached CO2 forms a readily hydrolyzable ester group; from an intermediate of the formula wherein R3 is a moiety that together with the attached CO2 forms a readily hydrolyzable ester group; Pg1 is an amino protecting group; R4 is H; or Pg1 can optionally be taken together with R4 and the nitrogen to which Pg1 and R4 are attached to form (i) an imine; or (ii) a fused or bridged bicyclic ring or a spirocyclic ring, wherein said ring is saturated and contains from 5 to 12 carbon atoms in which up to 2 carbon atoms are optionally replaced with a hetero moiety selected from O, S(O)j wherein j is an integer from 0 to 2, and —NR8—, provided that two O atoms, two S(O)j moieties, or an O atom and a S(O)j moiety are not attached directly to each other; R5 is selected from the group consisting of —C≡C— and —CH═CH—; and R8 is independently H or C1-C6 alkyl; to form the compound of the formula (I) that is optically pure; and to processes for preparing intermediates thereof.