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379260-71-6

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379260-71-6 Usage

General Description

Methyl 3-formyl-6-methoxy-1H-indole-2-carboxylate is a chemical compound with the molecular formula C13H11NO4. It is an ester of indole-2-carboxylic acid and is commonly used in organic synthesis and pharmaceutical research. METHYL 3-FORMYL-6-METHOXY-1H-INDOLE-2-CARBOXYLATE is a potential intermediate in the synthesis of various pharmaceuticals and biologically active molecules. It is also known for its unique chemical properties and has been the subject of various studies in the field of medicinal chemistry. Overall, Methyl 3-formyl-6-methoxy-1H-indole-2-carboxylate plays an important role as a building block in the development of new drugs and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 379260-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,9,2,6 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 379260-71:
(8*3)+(7*7)+(6*9)+(5*2)+(4*6)+(3*0)+(2*7)+(1*1)=176
176 % 10 = 6
So 379260-71-6 is a valid CAS Registry Number.

379260-71-6Downstream Products

379260-71-6Relevant articles and documents

COMPOSITIONS AND METHODS FOR ACTIVATING PYRUVATE KINASE

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Page/Page column 51-52; 56-57, (2022/02/05)

Provided herein are compositions and methods for activating pyruvate kinase (e.g., in a subject). In particular, provided herein are compositions and methods for treating a disease or condition (e.g., eye disease, blood disorders, or cancer) using pyruvate kinase activators.

Discovery of 3-Substituted 1H-Indole-2-carboxylic Acid Derivatives as a Novel Class of CysLT1 Selective Antagonists

Chen, Huayan,Yang, Hui,Wang, Zhilong,Xie, Xin,Nan, Fajun

supporting information, p. 335 - 339 (2016/03/25)

The indole derivative, 3-((E)-3-((3-((E)-2-(7-chloroquinolin-2yl)vinyl)phenyl)amino)-3-oxoprop-1-en-1-yl)-7-methoxy-1H-indole-2-carboxylic acid (17k), was identified as a novel and highly potent and selective CysLT1 antagonist with IC50 values of 0.0059 ± 0.0011 and 15 ± 4 μM for CysLT1 and CysLT2, respectively.

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