Cas 1359995-98-4,benzyl 4-ethyl-5-(3-formyl-1-azulenylmethyl)-3-methylpyrrole-2-carboxylate

1359995-98-4

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Basic information

Product Name: benzyl 4-ethyl-5-(3-formyl-1-azulenylmethyl)-3-methylpyrrole-2-carboxylate
Synonyms: benzyl 4-ethyl-5-(3-formyl-1-azulenylmethyl)-3-methylpyrrole-2-carboxylate
CAS NO:1359995-98-4
Molecular Formula:
Molecular Weight: 411.5
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: benzyl 4-ethyl-5-(3-formyl-1-azulenylmethyl)-3-methylpyrrole-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 4-ethyl-5-(3-formyl-1-azulenylmethyl)-3-methylpyrrole-2-carboxylate(1359995-98-4)
EPA Substance Registry System: benzyl 4-ethyl-5-(3-formyl-1-azulenylmethyl)-3-methylpyrrole-2-carboxylate(1359995-98-4)

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: 1359995-98-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1359995-98-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,9,9,9 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1359995-98:
(9*1)+(8*3)+(7*5)+(6*9)+(5*9)+(4*9)+(3*5)+(2*9)+(1*8)=244
244 % 10 = 4
So 1359995-98-4 is a valid CAS Registry Number.

1359995-98-4Upstream product

68-12-2 N,N-dimethyl-formamide

1359995-98-4Downstream Products

1359995-98-4Relevant academic research and scientific papers

Preparation of azulene-derived fulvenedialdehydes and their application to the synthesis of stable adj -dicarbaporphyrinoids

Lash, Timothy D.,Lammer, Aaron D.,Idate, Aparna S.,Colby, Denise A.,White, Kristen

, p. 2368 - 2381 (2012)

A "2 + 2" strategy for synthesizing adj-dicarbaporphyrinoid systems has been developed. In a model study, an azulenylmethylpyrrole dialdehyde was condensed with a dipyrrylmethane in the presence of HCl, followed by oxidation with ferric chloride, to give

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