Cas 1127303-65-4,3-Methyl-2-((2-(1E,2E)-(1,3,3-trimethylindolin-2-ylidene)ethylidene)amino)benzo[d]thiazol-3-ium iodide

1127303-65-4

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Basic information

Product Name: 3-Methyl-2-((2-(1E,2E)-(1,3,3-trimethylindolin-2-ylidene)ethylidene)amino)benzo[d]thiazol-3-ium iodide
Synonyms:
CAS NO:1127303-65-4
Molecular Formula:
Molecular Weight: 475.396
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: 3-Methyl-2-((2-(1E,2E)-(1,3,3-trimethylindolin-2-ylidene)ethylidene)amino)benzo[d]thiazol-3-ium iodide(CAS DataBase Reference)
NIST Chemistry Reference: 3-Methyl-2-((2-(1E,2E)-(1,3,3-trimethylindolin-2-ylidene)ethylidene)amino)benzo[d]thiazol-3-ium iodide(1127303-65-4)
EPA Substance Registry System: 3-Methyl-2-((2-(1E,2E)-(1,3,3-trimethylindolin-2-ylidene)ethylidene)amino)benzo[d]thiazol-3-ium iodide(1127303-65-4)

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: 1127303-65-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1127303-65-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,7,3,0 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1127303-65:
(9*1)+(8*1)+(7*2)+(6*7)+(5*3)+(4*0)+(3*3)+(2*6)+(1*5)=114
114 % 10 = 4
So 1127303-65-4 is a valid CAS Registry Number.

1127303-65-4Upstream product

84-83-3 (2E)-(1,3,3-trimethyl-1,3-dihydro-2H-indol-2-ylidene)acetaldehyde

1127303-65-4Downstream Products

1127303-65-4Relevant academic research and scientific papers

Reversible synthesis and characterization of dynamic imino analogues of trimethine and pentamethine cyanine dyes

Meguellati, Kamel,Spichty, Martin,Ladame, Sylvain

, p. 1123 - 1126 (2009)

A new family of unsymmetrical imine-based trimethine and pentamethine cyanine dye analogues is reported that can form under reversible and thermodynamically controlled conditions from non-or weakly emissive amine and aldehyde building blocks. These dynami

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