Cas 949680-17-5,(2-hydroxyphenyl)[5-(pyrrolidin-1-ylcarbonyl)-1H-pyrrol-3-yl]methanone

949680-17-5

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Basic information

Product Name: (2-hydroxyphenyl)[5-(pyrrolidin-1-ylcarbonyl)-1H-pyrrol-3-yl]methanone
Synonyms: (2-hydroxyphenyl)[5-(pyrrolidin-1-ylcarbonyl)-1H-pyrrol-3-yl]methanone
CAS NO:949680-17-5
Molecular Formula:
Molecular Weight: 284.315
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: (2-hydroxyphenyl)[5-(pyrrolidin-1-ylcarbonyl)-1H-pyrrol-3-yl]methanone(CAS DataBase Reference)
NIST Chemistry Reference: (2-hydroxyphenyl)[5-(pyrrolidin-1-ylcarbonyl)-1H-pyrrol-3-yl]methanone(949680-17-5)
EPA Substance Registry System: (2-hydroxyphenyl)[5-(pyrrolidin-1-ylcarbonyl)-1H-pyrrol-3-yl]methanone(949680-17-5)

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: 949680-17-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 949680-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,9,6,8 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 949680-17:
(8*9)+(7*4)+(6*9)+(5*6)+(4*8)+(3*0)+(2*1)+(1*7)=225
225 % 10 = 5
So 949680-17-5 is a valid CAS Registry Number.

949680-17-5Upstream product

949680-17-5Downstream Products

949680-17-5Relevant academic research and scientific papers

A synthesis of 5-hetaryl-3-(2-hydroxybenzoyl)pyrroles

Plaskon, Andrey S.,Ryabukhin, Sergey V.,Volochnyuk, Dmitriy M.,Shivanyuk, Alexander N.,Tolmachev, Andrey A.

, p. 5933 - 5943 (2008/09/21)

A facile and versatile procedure for the synthesis of 5-hetaryl-3-(2-hydroxybenzoyl)-1H-pyrroles and 4-(2-hydroxybenzoyl)-1H-pyrrole-2-carboxylic acid derivatives was established on the basis of TMSCl promoted recyclization of 3-formylchromone with various hetarylmethylamines and glycine derivatives.

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