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115186-31-7

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115186-31-7 Usage

Chemical Properties

White to off-white powder

Uses

Nalpha-Boc-Nepsilon-Fmoc-D-lysine is commonly used in the synthesis of aza-amino acids.

Check Digit Verification of cas no

The CAS Registry Mumber 115186-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,8 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 115186-31:
(8*1)+(7*1)+(6*5)+(5*1)+(4*8)+(3*6)+(2*3)+(1*1)=107
107 % 10 = 7
So 115186-31-7 is a valid CAS Registry Number.
InChI:InChI=1/C26H32N2O6/c1-26(2,3)34-25(32)28-22(23(29)30)14-8-9-15-27-24(31)33-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,21-22H,8-9,14-16H2,1-3H3,(H,27,31)(H,28,32)(H,29,30)/t22-/m1/s1

115186-31-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H62116)  Nalpha-Boc-Nepsilon-Fmoc-D-lysine, 95%   

  • 115186-31-7

  • 250mg

  • 329.0CNY

  • Detail
  • Alfa Aesar

  • (H62116)  Nalpha-Boc-Nepsilon-Fmoc-D-lysine, 95%   

  • 115186-31-7

  • 1g

  • 990.0CNY

  • Detail
  • Alfa Aesar

  • (H62116)  Nalpha-Boc-Nepsilon-Fmoc-D-lysine, 95%   

  • 115186-31-7

  • 5g

  • 3949.0CNY

  • Detail

115186-31-7SDS

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 Boc-D-Lys(Fmoc)-OH

1.2 Other means of identification

Product number -
Other names (2R)-6-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid

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:115186-31-7 SDS

115186-31-7Downstream Products

115186-31-7Relevant articles and documents

Solution phase synthesis of β-peptides using micro reactors

Watts, Paul,Wiles, Charlotte,Haswell, Stephen J,Pombo-Villar, Esteban

, p. 5427 - 5439 (2007/10/03)

The synthesis of β-peptides has been successfully performed using a borosilicate glass micro reactor, in which a network of channels has been produced using a photolithographic and wet etching method. The reagents were mobilised by electroosmotic flow (EOF). The micro reactor was initially evaluated using a carbodiimide coupling reaction to form a dipeptide. The methodology has been extended such that the peptides may also be produced via the pentafluorophenyl ester derivatives of amino acids. It was found that performing the pentafluorophenyl ester reactions in the micro reactor resulted in an increase in the reaction efficiency over the traditional batch method. We postulate that the enhancement in rate of reaction is an electrochemical phenomenon, due to the reaction being performed in an electric field, which is unique to micro reactor systems. It has also been demonstrated that selective deprotection of the resultant dipeptides can be achieved. This approach has been used in the synthesis of a tripeptide.

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