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
(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)
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.
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
