10309-14-5 Usage
Uses
Used in the Food Industry:
(Butylthio)acetic acid methyl ester is used as a flavoring agent for its distinct fruity and sulfurous aroma, enhancing the taste and smell of various food products.
Used in the Cosmetic Industry:
In the cosmetic sector, (Butylthio)acetic acid methyl ester is utilized as a fragrance ingredient, contributing to the creation of appealing scents in a variety of cosmetic products.
Used in the Pharmaceutical Industry:
(Butylthio)acetic acid methyl ester serves as a chemical intermediate in the production of pharmaceuticals, playing a crucial role in the synthesis of various medicinal compounds.
Used in the Agrochemical Industry:
(Butylthio)acetic acid methyl ester is also employed as a chemical intermediate in the agrochemical sector, where it is involved in the synthesis of different agrochemical products.
Used in the Synthesis of Bioactive Compounds:
(Butylthio)acetic acid methyl ester is used in the synthesis of bioactive compounds, which have potential applications in the fields of medicine and biotechnology, further expanding its utility and importance in scientific research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 10309-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,0 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10309-14:
(7*1)+(6*0)+(5*3)+(4*0)+(3*9)+(2*1)+(1*4)=55
55 % 10 = 5
So 10309-14-5 is a valid CAS Registry Number.
10309-14-5Relevant academic research and scientific papers
Reaction of methyl diazoacetate with aldehydes, amines, thiols, alcohols and acids over transition metal-exchanged clays
Phukan, Prodeep,Mohan, Jakkam Madan,Sudalai, Arumugam
, p. 3685 - 3689 (2007/10/03)
Metal-exchanged clays (M = Rh and Cu) catalyze effectively the reaction of methyl diazoacetate with various aldehydes, affording the corresponding β-keto esters in high yields. They have also been effective in the decomposition of methyl diazoacetate to form metallocarbenes which, in turn, successfully insert into X-H (X = N, O, S, CO2) bonds of a variety of amines, aldehydes, thiols and acids, thereby producing the corresponding esters. The Royal Society of Chemistry 1999.
Enzymatic resolution of α-acetoxysulfides: A new approach to the synthesis of homochiral S,O-acetals
Milton,Brand,Jones,Rayner
, p. 1903 - 1906 (2007/10/03)
A novel enzymatic resolution of α-acetoxysulfides using Pseudomonas fluorescens lipase is reported. Selectivity is highly dependent on the substrate and solvent, with enantiomeric excesses of >95% in some cases. We believe these are the first examples of enzymatic resolutions of an S,O-acetal.
A FACILE ROUTE TO HOMOCHIRAL SULFOXIDES
Burgess, Kevin,Henderson, Ian
, p. 3633 - 3636 (2007/10/02)
Biocatalytic resolution of methyl sulfinylacetates afford sulfoxides (R)-(1)-(6) in very high optical yields; the products have been used in a systematic study of the "SPAC" reaction, an asymmetric synthesis of γ-hydroxy-α,β-unsaturated esters.
