146137-98-6 Usage
Description
Methyl 4-methyl-1-benzothiophene-2-carboxylate is a chemical compound with the molecular formula C12H12O2S. It is a derivative of benzothiophene, a heterocyclic aromatic compound that contains a sulfur atom in the five-membered ring. methyl 4-methyl-1-benzothiophene-2-carboxylate is widely used in various industries, particularly as an intermediate in the synthesis of organic compounds and as a building block for biologically active molecules.
Uses
Used in Pharmaceutical Industry:
Methyl 4-methyl-1-benzothiophene-2-carboxylate is used as an intermediate in the synthesis of various organic compounds for pharmaceutical applications. Its unique structure and properties make it a valuable component in the development of new medications and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, methyl 4-methyl-1-benzothiophene-2-carboxylate is utilized as an intermediate for the synthesis of various compounds used in the development of pesticides, herbicides, and other agricultural chemicals. Its versatility in organic synthesis contributes to the creation of effective and targeted agrochemical products.
Used in Organic Synthesis:
Methyl 4-methyl-1-benzothiophene-2-carboxylate is used as a building block in organic synthesis for the preparation of biologically active molecules. Its presence in the molecular structure allows for the development of compounds with specific biological activities, making it an important component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medication Production:
As a key ingredient in the production of certain medications, methyl 4-methyl-1-benzothiophene-2-carboxylate plays a crucial role in the development and manufacturing of pharmaceutical products. Its incorporation into the molecular structure of these medications contributes to their therapeutic effects and overall efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 146137-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,1,3 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 146137-98:
(8*1)+(7*4)+(6*6)+(5*1)+(4*3)+(3*7)+(2*9)+(1*8)=136
136 % 10 = 6
So 146137-98-6 is a valid CAS Registry Number.
146137-98-6Relevant articles and documents
METHOD FOR PROMOTING PLANT GROWTH
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Paragraph 2113; 2114; 2115, (2015/10/28)
The present invention provides a method for promoting plant growth, which comprises treating a plant with a compound represented by the following Formula (1): provided that a method for promoting plant growth which comprises treating plants with a compound corresponding to any one of the following (1) to (8) is excluded: (1) Methyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (2) Methyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (3) Methyl 6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (4) Methyl 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (5) Ethyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (6) Ethyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (7) Ethyl 6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, and (8) Ethyl 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylate.
4-Substituted (benzo[b]thiophene-2-carbonyl)guanidines as novel Na +/H+ exchanger isoform-1 (NHE-1) inhibitors
Lee, Sunkyung,Lee, Hyunsuk,Kyu, Yang Yi,Byung, Ho Lee,Yoo, Sung-Eun,Lee, Kyunghee,Nam, Sook Cho
, p. 2998 - 3001 (2007/10/03)
A series of 4-substituted (benzo[b]thiophene-2-carbonyl)guanidines was synthesized and evaluated for the NHE-1 inhibitory activity and cardioprotective efficacy both in vitro and in vivo. Several analogs exhibited a strong inhibition on NHE-1, and which was generally well correlated with their cardioprotective efficacy. Especially the 4-nitro 20 and cyano 50 compounds excellently improved the cardiac function and reduced infarct size against ischemia/reperfusion injury.
UROKINASE INHIBITORS
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, (2008/06/13)
Disclosed are benzothiophene and thienothiophene derivatives useful for inhibiting urokinase activity.