Cas 1088976-74-2,6,6'-(1E,1'E)-(propane-1,3-diylbis(azan-1-yl-1-ylidene))bis(methan-1-yl-1-ylidene)bis(2,4-diiodophenol)

1088976-74-2

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Product Name: 6,6'-(1E,1'E)-(propane-1,3-diylbis(azan-1-yl-1-ylidene))bis(methan-1-yl-1-ylidene)bis(2,4-diiodophenol)
Synonyms: 6,6'-(1E,1'E)-(propane-1,3-diylbis(azan-1-yl-1-ylidene))bis(methan-1-yl-1-ylidene)bis(2,4-diiodophenol)
CAS NO:1088976-74-2
Molecular Formula:
Molecular Weight: 785.928
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: 6,6'-(1E,1'E)-(propane-1,3-diylbis(azan-1-yl-1-ylidene))bis(methan-1-yl-1-ylidene)bis(2,4-diiodophenol)(CAS DataBase Reference)
NIST Chemistry Reference: 6,6'-(1E,1'E)-(propane-1,3-diylbis(azan-1-yl-1-ylidene))bis(methan-1-yl-1-ylidene)bis(2,4-diiodophenol)(1088976-74-2)
EPA Substance Registry System: 6,6'-(1E,1'E)-(propane-1,3-diylbis(azan-1-yl-1-ylidene))bis(methan-1-yl-1-ylidene)bis(2,4-diiodophenol)(1088976-74-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1088976-74-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1088976-74-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,8,9,7 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1088976-74:
(9*1)+(8*0)+(7*8)+(6*8)+(5*9)+(4*7)+(3*6)+(2*7)+(1*4)=222
222 % 10 = 2
So 1088976-74-2 is a valid CAS Registry Number.

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1088976-74-2Relevant academic research and scientific papers

Synthesis, characterization, crystal structures and antibacterial activities of some Schiff bases with N2O2 donor sets

Ardakani, Amir Adabi,Kargar, Hadi,Feizi, Nourollah,Tahir, Muhammad Nawaz

, p. 1495 - 1504 (2018)

A series of Schiff base compounds were synthesized by the reaction of different 3,5-dihalosalicylaldehyde (halo atoms equal to Cl, Br and I) with polymethylenediamines of varying chain length. The Schiff bases were characterized using FT-IR, UV–Vis,

Design, synthesis, and pharmacological investigation of iodined salicylimines, new prototypes of antimicrobial drug candidates

Xu, Suo-Ping,Lv, Peng-Cheng,Shi, Lei,Zhu, Hai-Liang

, p. 282 - 290 (2011/07/08)

A series of 3,5-diiodo-salicylalidene Schiff bases (compounds 1 - 35) has been synthesized and tested for antimicrobial activity. The compounds were assayed for antibacterial activities by the MTT method. Some of the compounds inhibit the growth of a broad range of bacteria including the species of Bacillus subtilis, Staphylococcus aureus, Streptococcus faecalis, Pseudomonas aeruginosa, Escherichia coli, and Enterobacter cloacae. Among them, compounds 2-[(4-chloro-phenylimino)-methyl]-4,6-diiodo-phenol 11 and 2,4-diiodo-6-[(2- morpholin-4-yl-ethylimino)methyl]phenol 19 showed the most potent antibacterial activity with MIC of 3.1, 12.9, 3.3, 6.5, 12.9, 3.3 and 3.2, 12.8, 3.2, 12.8, 12.8, 3.2 μM against B. subtilis, S. aureus, S. faecalis, P. aeruginosa, E. Coli, and E. cloacae, respectively.

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