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benzyl (S)-N-[2-(1H-indol-3-yl)-1-phenylcarbamoylethyl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 158951-61-2 Structure
  • Basic information

    1. Product Name: benzyl (S)-N-[2-(1H-indol-3-yl)-1-phenylcarbamoylethyl]carbamate
    2. Synonyms: benzyl (S)-N-[2-(1H-indol-3-yl)-1-phenylcarbamoylethyl]carbamate
    3. CAS NO:158951-61-2
    4. Molecular Formula:
    5. Molecular Weight: 413.476
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 158951-61-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: benzyl (S)-N-[2-(1H-indol-3-yl)-1-phenylcarbamoylethyl]carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl (S)-N-[2-(1H-indol-3-yl)-1-phenylcarbamoylethyl]carbamate(158951-61-2)
    11. EPA Substance Registry System: benzyl (S)-N-[2-(1H-indol-3-yl)-1-phenylcarbamoylethyl]carbamate(158951-61-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 158951-61-2(Hazardous Substances Data)

158951-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158951-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,9,5 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 158951-61:
(8*1)+(7*5)+(6*8)+(5*9)+(4*5)+(3*1)+(2*6)+(1*1)=172
172 % 10 = 2
So 158951-61-2 is a valid CAS Registry Number.

158951-61-2Relevant articles and documents

Organocatalysis of asymmetric aldol reaction in water: Comparison of catalytic properties of (S)-valine and (S)-proline amides

Kucherenko,Siyutkin,Dashkin,Zlotin

, p. 1010 - 1015 (2014/03/21)

(S)-Valine amides containing (S)- or (R)-α-phenylethyl substituents at N1 atom efficiently catalyze asymmetric aldol reactions between cyclic (heterocyclic) ketones and aromatic aldehydes in water, predominantly giving rise to the aldol anti-di

Linear TMC-95-based proteasome inhibitors

Basse, Nicolas,Piguel, Sandrine,Papapostolou, David,Ferrier-Berthelot, Alexandra,Richy, Nicolas,Pagano, Maurice,Sarthou, Pierre,Sobczak-Thépot, Jo?lle,Reboud-Ravaux, Michele,Vidal, Jo?lle

, p. 2842 - 2850 (2008/02/07)

We have designed and evaluated 45 linear analogues of the natural constrained cyclopeptide TMC-95A. These synthetically less demanding molecules are based on the tripeptide sequence Y-N-W of TMC-95A. Structural variations in the amino acid side chains and

COMPOUNDS USEFUL AS MODULATORS OF THE PROTEASOME ACTIVITY

-

Page/Page column 33-34, (2008/06/13)

The present invention relates to the use of compounds of the following general formula (I): wherein no is 0 or 1, and when no is 1, X = CH2 or X = NCH2C6H5; R1 is OH, or a OR10 group, or a group of formula NH-(CH2)n1-R11; R2 is H, or an alkyl group, or a group of formula (CH2)n2-(CO)n3-NR13R14; R3 is H, or an alkyl group; R4 is H, or Boc, or Z; R5 is H, or Boc, or Z ; R6 is a OR16 group; R7 and R8 are H, or a halogen atom, as modulators of the proteasome activity, in the frame of the preparation of a medicament useful for the prevention or treatment of diseases wherein the proteasome is involved, or the preparation of cosmetic compositions, or of phytosanitary compositions.

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