Cas 889454-89-1,ethyl 4-(3-[{tetrahydropyran-2-yl}-oxy]-propyl)-5-methyl-2-phenyl-1-phenylpyrrole-3-carboxylate

889454-89-1

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Basic information

Product Name: ethyl 4-(3-[{tetrahydropyran-2-yl}-oxy]-propyl)-5-methyl-2-phenyl-1-phenylpyrrole-3-carboxylate
Synonyms: ethyl 4-(3-[{tetrahydropyran-2-yl}-oxy]-propyl)-5-methyl-2-phenyl-1-phenylpyrrole-3-carboxylate
CAS NO:889454-89-1
Molecular Formula:
Molecular Weight: 447.574
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: ethyl 4-(3-[{tetrahydropyran-2-yl}-oxy]-propyl)-5-methyl-2-phenyl-1-phenylpyrrole-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-(3-[{tetrahydropyran-2-yl}-oxy]-propyl)-5-methyl-2-phenyl-1-phenylpyrrole-3-carboxylate(889454-89-1)
EPA Substance Registry System: ethyl 4-(3-[{tetrahydropyran-2-yl}-oxy]-propyl)-5-methyl-2-phenyl-1-phenylpyrrole-3-carboxylate(889454-89-1)

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: 889454-89-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 889454-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,4,5 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 889454-89:
(8*8)+(7*8)+(6*9)+(5*4)+(4*5)+(3*4)+(2*8)+(1*9)=251
251 % 10 = 1
So 889454-89-1 is a valid CAS Registry Number.

889454-89-1Upstream product

62-53-3 aniline

889454-89-1Downstream Products

889454-89-1Relevant academic research and scientific papers

Synthesis of highly substituted pyrroles via a multimetal-catalyzed rearrangement-condensation-cyclization domino approach

Binder, Joerg T.,Kirsch, Stefan F.

, p. 2151 - 2153 (2006)

In a convenient one-pot process, easily accessed propargyl vinyl ethers and aromatic amines are effectively converted into tetra- and pentasubstituted 5-methylpyrroles which can further be transformed into 5-formylpyrroles via IBX-mediated oxidation. The

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