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35418-52-1

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35418-52-1 Usage

Definition

ChEBI: A hydroxamic acid resulting from the formal condensation of the primary amino group of N-(3-aminopropyl)-N-hydroxyacetamide (2 mol eq.) with the carboxy groups at positions 1 and 3 of citric acid. It is a siderophore p oduced by Bacillus megaterium and Anabaena species.

Check Digit Verification of cas no

The CAS Registry Mumber 35418-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35418-52:
(7*3)+(6*5)+(5*4)+(4*1)+(3*8)+(2*5)+(1*2)=111
111 % 10 = 1
So 35418-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H28N4O9/c1-11(21)19(28)7-3-5-17-13(23)9-16(27,15(25)26)10-14(24)18-6-4-8-20(29)12(2)22/h27-29H,3-10H2,1-2H3,(H,17,23)(H,18,24)(H,25,26)

35418-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name schizokinen

1.2 Other means of identification

Product number -
Other names 4-[3-[acetyl(hydroxy)amino]propylamino]-2-[2-[3-[acetyl(hydroxy)amino]propylamino]-2-oxoethyl]-2-hydroxy-4-oxobutanoic 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:35418-52-1 SDS

35418-52-1Downstream Products

35418-52-1Relevant articles and documents

Synthesis and iron coordination properties of schizokinen and its imide derivative

Chuljerm, Hataichanok,Chen, Yu-Lin,Srichairatanakool, Somdet,Hider, Robert C.,Cilibrizzi, Agostino

, p. 17395 - 17401 (2019/12/02)

The iron(iii) affinity constants for schizokinen and its imide derivative are reported for the first time. Surprisingly, schizokinen possesses a higher affinity for iron(iii) than desferrioxamine B; log?KFeIII (FeL), 36.2 and 30.6, respectively. This incr

Synthesis of Schizokinen, Homoschizokinen, Its Imide and the Detection of Imide with 13C-N.M.R.-Spectroscopy

Milewska, Maria J.,Chimiak, Andrzej,Glowacki, Zdzislaw

, p. 447 - 456 (2007/10/02)

A new method for the synthesis of homoschizokinen 1 and schizokinen 2 is described. 2-tert-Butyl-1,3-di-N-hydroxysuccinimidyl citrate has been applied as the key substrate.The method excludes the possibility of imide formation.The imide of compound 1 has

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