Cas 1103382-77-9,N,N,N-trimethyl-2-{4-[(E)-(4-propoxyphenyl)diazenyl]phenoxy}ethanaminium bromide

1103382-77-9

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Basic information

Product Name: N,N,N-trimethyl-2-{4-[(E)-(4-propoxyphenyl)diazenyl]phenoxy}ethanaminium bromide
Synonyms: N,N,N-trimethyl-2-{4-[(E)-(4-propoxyphenyl)diazenyl]phenoxy}ethanaminium bromide
CAS NO:1103382-77-9
Molecular Formula:
Molecular Weight: 422.365
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: N,N,N-trimethyl-2-{4-[(E)-(4-propoxyphenyl)diazenyl]phenoxy}ethanaminium bromide(CAS DataBase Reference)
NIST Chemistry Reference: N,N,N-trimethyl-2-{4-[(E)-(4-propoxyphenyl)diazenyl]phenoxy}ethanaminium bromide(1103382-77-9)
EPA Substance Registry System: N,N,N-trimethyl-2-{4-[(E)-(4-propoxyphenyl)diazenyl]phenoxy}ethanaminium bromide(1103382-77-9)

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: 1103382-77-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1103382-77-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,3,3,8 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1103382-77:
(9*1)+(8*1)+(7*0)+(6*3)+(5*3)+(4*8)+(3*2)+(2*7)+(1*7)=109
109 % 10 = 9
So 1103382-77-9 is a valid CAS Registry Number.

1103382-77-9Upstream product

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1103382-77-9Relevant academic research and scientific papers

Controlling molecular assembling by photons: Reversible light-powered monomer-aggregate interconversion of porphyrins

Callari, Fiorella L.,Sortino, Salvatore

supporting information; experimental part, p. 6179 - 6181 (2009/05/06)

Reversible formation and destruction of H-type aggregates of an anionic porphyrin can be controlled exclusively through light inputs of different energy exploiting the different interactions with the two isomeric forms of a cationic photoresponsive azobenzene-based surfactant. The Royal Society of Chemistry.

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