Cas 133345-51-4,2-((E)-1-(2-((E)-1-(2-hydroxyphenyl)ethylideneamino)phenylimino)ethyl)phenol

133345-51-4

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Basic information

Product Name: 2-((E)-1-(2-((E)-1-(2-hydroxyphenyl)ethylideneamino)phenylimino)ethyl)phenol
Synonyms: 2-((E)-1-(2-((E)-1-(2-hydroxyphenyl)ethylideneamino)phenylimino)ethyl)phenol
CAS NO:133345-51-4
Molecular Formula:
Molecular Weight: 344.413
EINECS: N/A
Product Categories: N/A
Mol File: 133345-51-4.mol
Article Data: 2

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: 2-((E)-1-(2-((E)-1-(2-hydroxyphenyl)ethylideneamino)phenylimino)ethyl)phenol(CAS DataBase Reference)
NIST Chemistry Reference: 2-((E)-1-(2-((E)-1-(2-hydroxyphenyl)ethylideneamino)phenylimino)ethyl)phenol(133345-51-4)
EPA Substance Registry System: 2-((E)-1-(2-((E)-1-(2-hydroxyphenyl)ethylideneamino)phenylimino)ethyl)phenol(133345-51-4)

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: 133345-51-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133345-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,4 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 133345-51:
(8*1)+(7*3)+(6*3)+(5*3)+(4*4)+(3*5)+(2*5)+(1*1)=104
104 % 10 = 4
So 133345-51-4 is a valid CAS Registry Number.

133345-51-4Upstream product

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133345-51-4Relevant articles and documents

Synthesis and antibacterial studies of some reduced schiff base derivatives

Patil, Udaysinha,Khan, Asif,Nagarsekar, Aarti,Mandewale, Mustapha,Yamgar, Ramesh

, p. 2796 - 2805 (2019/01/05)

A series of N,N-substituted ethylene-1,2-diamine derivatives have been prepared from reaction of 2-hydroxybenzaldehyde derivatives and 1,2-diamine derivatives in the presence of NaBH4 through Schiff base intermediate. The synthesized compounds were screened for their antibacterial activities. Compound SB01, SB02 and SB09 displayed significant activity at MIC ranges from 0.40-6.25 μg/mL.

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