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130304-80-2

130304-80-2

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130304-80-2 Usage

Chemical Properties

White to off-white crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 130304-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,3,0 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 130304-80:
(8*1)+(7*3)+(6*0)+(5*3)+(4*0)+(3*4)+(2*8)+(1*0)=72
72 % 10 = 2
So 130304-80-2 is a valid CAS Registry Number.
InChI:InChI=1/C25H27NO6/c27-23(28)14-22(24(29)32-16-8-2-1-3-9-16)26-25(30)31-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,16,21-22H,1-3,8-9,14-15H2,(H,26,30)(H,27,28)

130304-80-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H66639)  N-Fmoc-L-aspartic acid 4-cyclohexyl ester, 95%   

  • 130304-80-2

  • 5g

  • 753.0CNY

  • Detail

  • Alfa Aesar

  • (H66639)  N-Fmoc-L-aspartic acid 4-cyclohexyl ester, 95%   

  • 130304-80-2

  • 25g

  • 3009.0CNY

  • Detail

130304-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-4-cyclohexyloxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names AmbotzFAA1705

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:130304-80-2 SDS

130304-80-2Upstream product

130304-80-2Downstream Products

130304-80-2Relevant articles and documents

MgI2-chemoselective cleavage for removal of amino acid protecting groups: A fresh vision for peptide synthesis

Berthet, Mathéo,Martinez, Jean,Parrot, Isabelle

, (2017)

In the field of peptide synthesis, the key to a successful access to synthetic targets lies on a pertinent combination of protecting groups. Their choice is directed by their selective removal conditions. We present here the behavior of some of the most used protecting groups in peptide chemistry under experimental cleavage conditions, combining MgI2 with MW irradiation, using 2-Me-THF as a green solvent. In these experimental conditions, the benzyloxycarbonyl protecting group as well as the Merrifield resin can be re-considered in peptide chemistry.

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