57678-46-3 Usage
Uses
Used in Pharmaceutical Industry:
5-OXO-5,6,7,8-TETRAHYDRONAPHTHALENE-2-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 5-OXO-5,6,7,8-TETRAHYDRONAPHTHALENE-2-CARBOXYLIC ACID is utilized as a building block for the creation of new agrochemicals, potentially enhancing crop protection and yield.
Used in Material Science:
5-OXO-5,6,7,8-TETRAHYDRONAPHTHALENE-2-CARBOXYLIC ACID is employed in material science as a component in the development of novel materials, leveraging its chemical structure to improve material properties.
Used in Organic Synthesis:
As a versatile organic compound, 5-OXO-5,6,7,8-TETRAHYDRONAPHTHALENE-2-CARBOXYLIC ACID is used as a synthetic building block for the preparation of a wide range of organic compounds, contributing to the advancement of organic chemistry and its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 57678-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,7 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57678-46:
(7*5)+(6*7)+(5*6)+(4*7)+(3*8)+(2*4)+(1*6)=173
173 % 10 = 3
So 57678-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2/c1-11(2)9-5-3-4-8(6-9)7-10/h3-6H,7,10H2,1-2H3
57678-46-3Relevant academic research and scientific papers
Synthesis and activity of N-oxalylglycine and its derivatives as Jumonji C-domain-containing histone lysine demethylase inhibitors
Hamada, Shohei,Kim, Tae-Dong,Suzuki, Takayoshi,Itoh, Yukihiro,Tsumoto, Hiroki,Nakagawa, Hidehiko,Janknecht, Ralf,Miyata, Naoki
scheme or table, p. 2852 - 2855 (2010/07/03)
N-Oxalylglycine (NOG) derivatives were synthesized, and their inhibitory effect on histone lysine demethylase activity was evaluated. NOG and compound 1 inhibited histone lysine demethylases JMJD2A, 2C and 2D in enzyme assays, and their dimethyl ester prodrugs DMOG and 21 exerted histone lysine methylating activity in cellular assays.
(3-HYDROXY-4-AMINO-BUTAN-2-YL) -3- (2-THIAZOL-2-YL-PYRROLIDINE-1-CARBONYL) BENZAMIDE DERIVATIVES AND RELATED COMPOUNDS AS BETA-SECRETASE INHIBITORS FOR TREATING
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Page/Page column 85, (2009/05/29)
The present invention provides novel beta-secretase inhibitors and methods for their use, including methods of treating of Alzheimer's disease. (Formula)
The antiinfluenza activity of pyrrolo[2,3-d]pyrimidines
Sznaidman, Marcos L.,Meade, Eric A.,Beauchamp, Lilia M.,Russell, Stuart,Tisdale, Margaret
, p. 565 - 568 (2007/10/03)
From a group of pyrrolo[2,3-d]pyrimidine compounds that have been screened against influenza virus, one derivative, 4-(3-piperidinyl benzylamino)-2-methyl-7H-pyrrolo[2,3-d]pyrimidine (9), has shown promising activity against both the A and B strains. The
