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THIOGLYCOLIC ACID N-BUTYL ESTER, also known as Butyl mercaptoacetate, is an organic compound that is characterized by its unique chemical structure and properties. It is a derivative of thioglycolic acid, with a butyl group attached to the ester functional group. THIOGLYCOLIC ACID N-BUTYL ESTER is known for its reactivity and versatility in various chemical reactions and applications.

10047-28-6

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10047-28-6 Usage

Uses

Used in Pharmaceutical Industry:
THIOGLYCOLIC ACID N-BUTYL ESTER is used as a synthetic intermediate for the production of various pharmaceutical compounds. Its unique chemical structure allows it to be a key component in the synthesis of drugs with specific therapeutic properties.
Used in Chemical Synthesis:
In the field of chemical synthesis, THIOGLYCOLIC ACID N-BUTYL ESTER is used as a reagent in various organic reactions. Its ability to participate in a wide range of reactions makes it a valuable tool for chemists in creating new compounds with desired properties.
Used in Cu-Catalyzed Denitrogenative Transannulation:
THIOGLYCOLIC ACID N-BUTYL ESTER is used as a reactant in the Cu-Catalyzed Denitrogenative Transannulation of 3-Aminoindazoles to assemble 1-Aminoisoquinolines and 3-Aminobenzothiophenes. This application highlights its importance in the synthesis of complex organic molecules, which can be further utilized in various industries, including pharmaceuticals and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 10047-28-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,4 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10047-28:
(7*1)+(6*0)+(5*0)+(4*4)+(3*7)+(2*2)+(1*8)=56
56 % 10 = 6
So 10047-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2S/c1-2-3-4-9-6(8)5-7/h7H,2-5H2,1H3

10047-28-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Butyl Thioglycolate

1.2 Other means of identification

Product number -
Other names Mercaptoacetic Acid Butyl Ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10047-28-6 SDS

10047-28-6Relevant academic research and scientific papers

The reaction of condensation of furfural with mercaptoacetic acid esters

Asadova,Guseinov,Allakhverdiev

, p. 787 - 789 (2013/07/26)

The condensation reaction of furfural with various mercaptoacetic acid esters was studied. The reaction products were tested for their corrosion protective properties in M-16 cylinder oil used for marine diesel engines. It was found that the resulting 2-d

Pesticidal compositions containing phosphoric esters and divalent sulphur compounds

-

, (2008/06/13)

Pesticidal composition comprising: a pesticidal, phosphoric ester the molecule of which has at least one alkyl group of 1 to 3 carbon atoms, 0.05 to 10% of an agent stabilizing the said ester against decomposition by protonisation, together with adjuvants characterized in that the stabilizing agent comprises at least one sulphur compound containing per molecule at least one divalent sulphur atom of which one valence is bonded to an atom chosen from sulphur, carbon, nitrogen, hydrogen, and metals capable of giving a salt, the other valence being bonded to an atom chosen from hydrogen, the carbon atom already noted, a second carbon atom, the nitrogen atom already noted, a second nitrogen atom, the metal atom already noted in the case of a metal of valence greater than one, a second atom of metal and oxygen when the first valence is not attached to an atom of hydrogen, the proportion of sulphur calculated with reference to the weight of the sulphur compound being between 5 and 99%. Process for stabilizing a phosphoric ester of which the molecule possesses at least one alkyl group containing 1 to 3 carbon atoms characterized in that there is added to the phosphoric ester or to a mixture which contains it, 0.05 to 10% calculated on the weight of the phosphoric acid ester of an agent capable of stabilizing the said phosphoric ester against protonisation and comprising at least one sulphur compound such as that defined thereupon.

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