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4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150618-07-8

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150618-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150618-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,6,1 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 150618-07:
(8*1)+(7*5)+(6*0)+(5*6)+(4*1)+(3*8)+(2*0)+(1*7)=108
108 % 10 = 8
So 150618-07-8 is a valid CAS Registry Number.

150618-07-8Downstream Products

150618-07-8Relevant academic research and scientific papers

Selective inhibition of Src SH2 by a novel thiol-targeting tricarbonyl-modified inhibitor and mechanistic analysis by 1H/13C NMR spectroscopy

Sundaramoorthi, Raji,Siedem, Chris,Vu, Chi B.,Dalgarno, David C.,Laird, Ellen C.,Botfield, Martyn C.,Combs, Amanda B.,Adams, Susan E.,Yuan, Ruth W.,Weigele, Manfred,Narula, Surinder S.

, p. 1665 - 1669 (2007/10/03)

Detailed analysis of Src SH2 binding by peptides containing a novel tricarbonyl-modified pTyr moiety is described. We envisaged that Src SH2 selectivity might be obtained by exploiting the thiol group of Cys188 present in the pTyr binding pocket of the pr

A synthetic receptor for the Cbz-L-Ala-L-Ala-OH dipeptide sequence

Henley, Peter D.,Kilburn, Jeremy D.

, p. 1335 - 1336 (2007/10/03)

A novel bowl-shaped macrobicyclic receptor has been prepared and is a particularly strong and selective receptor for Cbz-L-Ala-L-Ala-OH(-ΔG(ass) = 25 kJ mol-1 at 293 K in CDCL3).

Preparation of L-(Phosphonodifluoromethyl) phenylalanine derivatives as non-hydrolyzable mimetics of O-phosphotyrosine

Wrobel, Jay,Dietrich, Arlene

, p. 3543 - 3546 (2007/10/02)

N-t-BOC-L-(Phosphonodifluoromethyl)phenylalanine benzyl ester (1) was prepared in 5 steps from N-t-BOC-L-tyrosine benzyl eser O-triflate (4). Compound 1 was further converted to derivatives 2 and 3 which are potentially suitable for peptide synthesis. Ana

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