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127902-98-1

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  • Butanedioic acid,2-[2-[[(1R)-1-carboxy-4-[[(3S)-3,4-dicarboxy-3-hydroxy-1-oxobutyl]amino]butyl]amino]-2-oxoethyl]-2-hydroxy-,(2S)-

    Cas No: 127902-98-1

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127902-98-1 Usage

Definition

ChEBI: A D-ornithine derivative obtained by formal condensation of the terminal carboxy groups of two citric acid units with the two amino groups of D-ornithine.

Check Digit Verification of cas no

The CAS Registry Mumber 127902-98-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,0 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 127902-98:
(8*1)+(7*2)+(6*7)+(5*9)+(4*0)+(3*2)+(2*9)+(1*8)=141
141 % 10 = 1
So 127902-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H24N2O14/c20-9(4-16(32,14(28)29)6-11(22)23)18-3-1-2-8(13(26)27)19-10(21)5-17(33,15(30)31)7-12(24)25/h8,32-33H,1-7H2,(H,18,20)(H,19,21)(H,22,23)(H,24,25)(H,26,27)(H,28,29)(H,30,31)

127902-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name staphyloferrin A

1.2 Other means of identification

Product number -
Other names 2-[2-[[4-carboxy-4-[(3,4-dicarboxy-3-hydroxybutanoyl)amino]butyl]amino]-2-oxoethyl]-2-hydroxybutanedioic 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:127902-98-1 SDS

127902-98-1Downstream Products

127902-98-1Relevant articles and documents

Streamlined synthesis of (R, R)-rhizoferrin, (S, S)-rhizoferrin and (R, S, R)-staphyloferrin A

Csuk, René,Deising, Holger B.,Raschke, Anja,Serbian, Immo,Wiese, Jana

, p. 64 - 69 (2019)

(R, R)-Rhizoferrin and (R, S, R)-staphyloferrin A are carboxylate-type siderophores. Their streamlined synthesis has been accomplished starting from (R)-citric acid. Key-step of these syntheses is a chemo-enzymatic ester hydrolysis. (S, S)-rhizoferrin was accessible by a multistep synthesis starting from an (S)-citrate derived synthon.

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