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methyl N-(tert-butoxycarbonyl)tryptophylisoleucinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72156-60-6

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72156-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72156-60-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,1,5 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72156-60:
(7*7)+(6*2)+(5*1)+(4*5)+(3*6)+(2*6)+(1*0)=116
116 % 10 = 6
So 72156-60-6 is a valid CAS Registry Number.

72156-60-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-[[3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]amino]-3-methylpentanoate

1.2 Other means of identification

Product number -
Other names MeO-Ile-Trp-Boc

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:72156-60-6 SDS

72156-60-6Relevant academic research and scientific papers

Solvent-free peptide synthesis assisted by microwave irradiation: Environmentally benign synthesis of bioactive peptides

Mahindra, Amit,Patel, Neha,Bagra, Nitin,Jain, Rahul

, p. 3065 - 3069 (2014/01/06)

An efficient and facile, solvent-free peptide synthesis assisted by microwave irradiation, using DIC/HONB as the coupling reagent combination is reported. Key features of this original protocol are solvent-free synthesis, very short reaction time and scal

Microwave-assisted solution phase peptide synthesis in neat water

Mahindra, Amit,Nooney, Karthik,Uraon, Shrikant,Sharma, Krishna K.,Jain, Rahul

, p. 16810 - 16816 (2013/09/23)

An environmentally benign protocol for solution phase peptide synthesis has been developed in neat water using TBTU/HOBt/DIEA as a coupling combination under microwave irradiation. Key features of this procedure are the replacement of commonly used toxic organic solvents like DMF and NMP, the use of lower amounts of reactants, compatibility with both N-α-Boc- and N-α-Fmoc-protected amino acids and all commonly used side-chain protective groups, short reaction time, and racemization-free synthesis in high yield and purity. The Royal Society of Chemistry 2013.

Histone deacetylase inhibitors: Synthesis of cyclic tetrapeptides and their triazole analogs

Singh, Erinprit K.,Nazarova, Lidia A.,Lapera, Stephanie A.,Alexander, Leslie D.,McAlpine, Shelli R.

supporting information; experimental part, p. 4357 - 4360 (2010/09/12)

Synthesis of nine macrocyclic peptide HDAC inhibitors and three triazole derivatives is described. HDAC inhibitory activity of these compounds against HeLa cell lysate is evaluated. The biological data demonstrate that incorporation of a triazole unit improves the HDAC inhibitory activity.

Copper-catalyzed cyclization of lodo-tryptophans: A straightforward synthesis of pyrroloindoles

Coste, Alexis,Toumi, Mathieu,Wright, Karen,Razafimahaleo, Vanessa,Couty, Francois,Marrot, Jerome,Evano, Gwilherm

supporting information; experimental part, p. 3841 - 3844 (2009/07/01)

(Chemical Equation Presented) Pyrroloindoles are a key structural motif found in a wide number of biologically active alkaloids. Intramolecular copper-catalyzed coupling of readily accessible 2-iodo-tryptophan derivatives occurs in excellent yield, afford

Selective inhibitors of the serine protease plasmin: Probing the S3 and S3′ subsites using a combinatorial library

Xue, Fengtian,Seto, Christopher T.

, p. 6908 - 6917 (2007/10/03)

A combinatorial library of 400 serine protease inhibitors with the general structure Cbz-Xaa-Trp-cyclohexanone-Trp-Yaa-OH has been constructed. The library was synthesized on the solid phase using mix-and-split synthesis, where 20 di

Synthesis of endothiopeptides and their cyclization to 1,3-thiazol- 5(4H)-imines

Lehmann, Juerg,Heimgartner, Heinz

, p. 1899 - 1915 (2007/10/03)

Further investigations of the synthesis of endothio analogues of the segment 1-10 (8) of an apolar analogon of zervamicin IIA are described. The endothiodecapeptide Boc-Trp-Ile-Ala-Aib-Ile-Val-Aib-Leu-Aib-Ψ(CS)-Pro-OMe (10) has been prepared in good yield

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