Cas 130296-41-2,N<sup>1</sup>,N<sup>2</sup>-Bis(2,5-di-tert-butylphenyl)-3-amino-4,9,10-perylentricarbonsaeure-3,4-lactam-9,10-imid

130296-41-2

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Basic information

Product Name: N¹,N²-Bis(2,5-di-tert-butylphenyl)-3-amino-4,9,10-perylentricarbonsaeure-3,4-lactam-9,10-imid
Synonyms: N¹,N²-Bis(2,5-di-tert-butylphenyl)-3-amino-4,9,10-perylentricarbonsaeure-3,4-lactam-9,10-imid
CAS NO:130296-41-2
Molecular Formula:
Molecular Weight: 738.97
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: N¹,N²-Bis(2,5-di-tert-butylphenyl)-3-amino-4,9,10-perylentricarbonsaeure-3,4-lactam-9,10-imid(CAS DataBase Reference)
NIST Chemistry Reference: N¹,N²-Bis(2,5-di-tert-butylphenyl)-3-amino-4,9,10-perylentricarbonsaeure-3,4-lactam-9,10-imid(130296-41-2)
EPA Substance Registry System: N¹,N²-Bis(2,5-di-tert-butylphenyl)-3-amino-4,9,10-perylentricarbonsaeure-3,4-lactam-9,10-imid(130296-41-2)

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: 130296-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130296-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,9 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130296-41:
(8*1)+(7*3)+(6*0)+(5*2)+(4*9)+(3*6)+(2*4)+(1*1)=102
102 % 10 = 2
So 130296-41-2 is a valid CAS Registry Number.

130296-41-2Upstream product

83054-80-2 N,N'-bis(2,5-di-tert-butylphenyl)perylene-3,4:9,10-bis(dicarboximide)

130296-41-2Downstream Products

130296-41-2Relevant academic research and scientific papers

Synthesis of Nonsymmetrically Substituted Perylene Fluorescent Dyes

Kaiser, Harald,Lindner, Joerg,Langhals, Heinz

, p. 529 - 535 (2007/10/02)

A general method for the preparation of perylene-3,4:9,10-tetracarboxdiimides 1 with two different substituents at the nitrogen atoms is described: The easily prepared symmetrical tetracarboxdiimides 1 (R1=R2) are transformed into carboxdiimide anhydrides 2 and condensed with primary amines to the corresponding tetracarboxdiimides 1 (R1 R2).Applications as fluorescent tracers in biochemistry and polymer chemistry are discussed.

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