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(S)-tert-butyl (2-(methylthio)-1-phenylethyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

171002-00-9

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171002-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171002-00-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,0,0 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 171002-00:
(8*1)+(7*7)+(6*1)+(5*0)+(4*0)+(3*2)+(2*0)+(1*0)=69
69 % 10 = 9
So 171002-00-9 is a valid CAS Registry Number.

171002-00-9Downstream Products

171002-00-9Relevant academic research and scientific papers

NOVEL COMPOUNDS THAT ARE ERK INHIBITORS

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Paragraph 0342, (2018/04/20)

Disclosed are the ERK inhibitors of formula (1): and the pharmaceutically acceptable salts thereof. Also disclosed are methods of treating cancer using the compounds of formula (1).

NOVEL COMPOUNDS THAT ARE ERK INHIBITORS

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Page/Page column 92, (2013/05/21)

Disclosed are the ERK inhibitors of formula (1): and the pharmaceutically acceptable salts thereof. Also disclosed are methods of treating cancer using the compounds of formula (1)

BICYCLIC HETEROCYCLE DERIVATIVES AND USE THEREOF AS GPR119 MODULATORS

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Page/Page column 179-180, (2009/12/27)

The present invention relates to Bicyclic Heterocycle Derivatives of formula (I), compositions comprising a Bicyclic Heterocycle Derivative, and methods of using the Bicyclic Heterocycle Derivatives for treating or preventing obesity, diabetes, a metabolic disorder, a cardiovascular disease or a disorder related to the activity of GPR1 19 in a patient.

Synthesis of chiral β-amino sulfides and β-amino thiols from α-amino acids

Cran,Gibson,Handa

, p. 1553 - 1556 (2007/10/02)

Bifurcated routes to two series of chiral secondary β-amino sulfides 5a-c and 11a-c have been developed from L-proline and (S)-phenylglycine, respectively. The developed methodology had also led to the synthesis of the tertiary β-amino thiol 7 and the primary β-amino sulfide 12 from L-proline and (S)-phenylglycine, respectively.

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