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4-methyl-5-nitro-2-phenoxy-pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

935877-74-0

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935877-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 935877-74-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,8,7 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 935877-74:
(8*9)+(7*3)+(6*5)+(5*8)+(4*7)+(3*7)+(2*7)+(1*4)=230
230 % 10 = 0
So 935877-74-0 is a valid CAS Registry Number.

935877-74-0Downstream Products

935877-74-0Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS FOR THE TREATMENT OF EPILEPSY

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Paragraph 0134; 0143; 0144, (2020/06/19)

The present invention provides a novel heterocyclic compound represented by Formula [I] and a salt thereof: wherein the symbols are as defined in the specification, which is useful for treating, preventing and/or diagnosing seizure and the like in disease involving epileptic seizure or convulsive seizure (including multiple drug resistant seizure, refractory seizure, acute symptomatic seizure, febrile seizure and status epilepticus), as well as a medical use therefor.

INHIBITORS OF BRUTON'S TYROSINE KINASE

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Page/Page column 59; 63; 65, (2015/06/25)

This application discloses compounds according to generic Formula (I) wherein all variables are defined as described herein, which inhibit Btk. The compounds disclosed herein are useful to modulate the activity of Btk and treat diseases associated with ex

2-AMINO-3,4-DIHYDRO-PYRIDO[3,4-D]PYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF BETA-SECRETASE (BACE)

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Page/Page column 79, (2008/06/13)

The present invention is directed to 2-amino-3,4-dihydro-pyrido[3,4-d]pyrimidine derivatives of formula (I), pharmaceutical compositions containing them and their use in the treatment of Alzheimer's disease (AD) and related disorders. The compounds of the invention are inhibitors of β-site cleaving enzyme and BACE, BACE1, Asp2 and memapsin2.

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