122308-25-2 Usage
Description
DIMETHYL 2-(THIOPHEN-2-YLMETHYL)MALONATE is a chemical compound with the molecular formula C11H12O4S. It is a clear liquid with a slightly fruity odor and is commonly used as an intermediate in organic synthesis.
Uses
Used in Pharmaceutical Industry:
DIMETHYL 2-(THIOPHEN-2-YLMETHYL)MALONATE is used as an intermediate in the production of pharmaceuticals for its ability to contribute to the synthesis of various medicinal compounds.
Used in Agrochemical Industry:
DIMETHYL 2-(THIOPHEN-2-YLMETHYL)MALONATE is used as an intermediate in the production of agrochemicals, playing a role in the development of substances for agricultural applications.
Used in Dye Industry:
DIMETHYL 2-(THIOPHEN-2-YLMETHYL)MALONATE is used as a component in the manufacturing of dyes, contributing to the creation of diverse colorants for various industries.
Used in Perfume and Flavor Industry:
DIMETHYL 2-(THIOPHEN-2-YLMETHYL)MALONATE is used as a building block for creating perfumes and flavors, enhancing the aromatic profiles of these products.
Used in Material Science:
DIMETHYL 2-(THIOPHEN-2-YLMETHYL)MALONATE is used in the development of new materials, serving as a versatile building block for innovative applications.
Used in Organic Synthesis:
DIMETHYL 2-(THIOPHEN-2-YLMETHYL)MALONATE is used as a key intermediate in organic synthesis, enabling the construction of more complex organic compounds for various purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 122308-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,0 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122308-25:
(8*1)+(7*2)+(6*2)+(5*3)+(4*0)+(3*8)+(2*2)+(1*5)=82
82 % 10 = 2
So 122308-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O4S/c1-13-9(11)8(10(12)14-2)6-7-4-3-5-15-7/h3-5,8H,6H2,1-2H3
122308-25-2Relevant articles and documents
Reductive Knoevenagel Condensation with the Zn-AcOH System
Ivanov, Konstantin L.,Melnikov, Mikhail Ya.,Budynina, Ekaterina M.
, p. 1285 - 1291 (2021)
An efficient gram-scale one-pot approach to 2-substituted malonates and related structures is developed, starting from commercially available aldehydes and active methylene compounds. The technique combines Knoevenagel condensation with the reduction of the C=C bond in the resulting activated alkenes with the Zn-AcOH system. The relative ease with which the C=C bond reduction occurs can be traced to the accepting abilities of the substituents in the intermediate arylidene malonates.
