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3-[[(1S)-5-(acetyl-hydroxy-amino)-1-carboxy-pentyl]carbamoyl]-2-[[(1S)-5-(acetyl-hydroxy-amino)-1-carboxy-pentyl]carbamoylmethyl]-2-hydroxy-propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26198-65-2

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26198-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26198-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,9 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26198-65:
(7*2)+(6*6)+(5*1)+(4*9)+(3*8)+(2*6)+(1*5)=132
132 % 10 = 2
So 26198-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H36N4O13/c1-13(27)25(38)9-5-3-7-15(19(31)32)23-17(29)11-22(37,21(35)36)12-18(30)24-16(20(33)34)8-4-6-10-26(39)14(2)28/h15-16,37-39H,3-12H2,1-2H3,(H,23,29)(H,24,30)(H,31,32)(H,33,34)(H,35,36)/t15-,16-/m0/s1

26198-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name aerobactin

1.2 Other means of identification

Product number -
Other names -

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:26198-65-2 SDS

26198-65-2Downstream Products

26198-65-2Relevant academic research and scientific papers

Utilizing an iron(III)-chelation masking strategy to prepare mono- and bis-functionalized aerobactin analogues for targeting pathogenic bacteria

Ho, Yu-Hin,Ho, Sheng-Yang,Hsu, Cheng-Chih,Shie, Jiun-Jie,Wang, Tsung-Shing Andrew

, p. 9265 - 9268 (2017)

A direct and selective method for the functionalization of aerobactin has been described. Selectivity was achieved by masking the functioning carboxylate via iron-chelation, leaving the two remaining carboxylates for direct modification. Both mono- and bis-functionalized aerobactin effectively targeted pathogenic bacteria, showing a facile method with prospective applications.

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