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103185-30-4

fluvibactin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103185-30-4

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103185-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103185-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,8 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103185-30:
(8*1)+(7*0)+(6*3)+(5*1)+(4*8)+(3*5)+(2*3)+(1*0)=84
84 % 10 = 4
So 103185-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C31H34N4O10/c1-17-24(34-30(45-17)20-9-4-12-23(38)27(20)41)31(44)35(15-5-13-32-28(42)18-7-2-10-21(36)25(18)39)16-6-14-33-29(43)19-8-3-11-22(37)26(19)40/h2-4,7-12,17,24,34,36-40H,5-6,13-16H2,1H3,(H,32,42)(H,33,43)/b30-20-

103185-30-4SDS

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 (2Z)-N,N-bis[3-[(2,3-dihydroxybenzoyl)amino]propyl]-2-(5-hydroxy-6-oxocyclohexa-2,4-dien-1-ylidene)-5-methyl-1,3-oxazolidine-4-carboxamide

1.2 Other means of identification

Product number -
Other names N(4)-(2-(2,3-Dihydroxyphenyl)-5-methyl-2-oxazolin-4-yl)carboxy-N(1),N(7)-bis(2,3-dihydroxybenzoyl)norspermidine

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:103185-30-4 SDS

103185-30-4Downstream Products

103185-30-4Relevant articles and documents

Convergent total syntheses of fluvibactin and vibriobactin using molybdenum(vi) oxide-catalyzed dehydrative cyclization as a key step

Sakakura, Akira,Umemura, Shuhei,Ishihara, Kazuaki

supporting information; experimental part, p. 3561 - 3563 (2009/02/05)

Efficient total syntheses of fluvibactin and vibriobactin have been achieved via molybdenum(vi) oxide-catalyzed dehydrative cyclization, Sb(OEt)3-catalyzed ester-amide transformation, and WSCI and HOAt-promoted dehydrative amide formation. The Royal Society of Chemistry.

Significance of asymmetric sites in choosing siderophores as deferration agents

Bergeron,Mei Gou Xin,Weimar,Smith,Wiegand

, p. 2469 - 2478 (2007/10/03)

The syntheses of the microbial iron chelators L-fluviabactin, its unnatural enantiomer, D-fluviabactin, L-homofluviabactin, and L-agrobactin, are described. The key steps involve the selective bis-acylation of the terminal nitrogens of norspermidine, sper

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