Cas 357628-48-9,N5-(N-carbobenzyloxy-L-threonyl)-N1,N9-bis[2,3-bis(benzyloxy)benzoyl]homospermidine

357628-48-9

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Basic information

Product Name: N⁵-(N-carbobenzyloxy-L-threonyl)-N¹,N⁹-bis[2,3-bis(benzyloxy)benzoyl]homospermidine
Synonyms: N⁵-(N-carbobenzyloxy-L-threonyl)-N¹,N⁹-bis[2,3-bis(benzyloxy)benzoyl]homospermidine
CAS NO:357628-48-9
Molecular Formula:
Molecular Weight: 1027.23
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N⁵-(N-carbobenzyloxy-L-threonyl)-N¹,N⁹-bis[2,3-bis(benzyloxy)benzoyl]homospermidine(CAS DataBase Reference)
NIST Chemistry Reference: N⁵-(N-carbobenzyloxy-L-threonyl)-N¹,N⁹-bis[2,3-bis(benzyloxy)benzoyl]homospermidine(357628-48-9)
EPA Substance Registry System: N⁵-(N-carbobenzyloxy-L-threonyl)-N¹,N⁹-bis[2,3-bis(benzyloxy)benzoyl]homospermidine(357628-48-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 357628-48-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 357628-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,6,2 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 357628-48:
(8*3)+(7*5)+(6*7)+(5*6)+(4*2)+(3*8)+(2*4)+(1*8)=179
179 % 10 = 9
So 357628-48-9 is a valid CAS Registry Number.

357628-48-9Upstream product

357628-48-9Downstream Products

357628-48-9Relevant academic research and scientific papers

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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