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1-Pentanone, 4-methyl-4-nitro-1-phenyl-3-(4-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74362-00-8

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74362-00-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74362-00-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,6 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74362-00:
(7*7)+(6*4)+(5*3)+(4*6)+(3*2)+(2*0)+(1*0)=118
118 % 10 = 8
So 74362-00-8 is a valid CAS Registry Number.

74362-00-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-4-nitro-1-phenyl-3-pyridin-4-ylpentan-1-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:74362-00-8 SDS

74362-00-8Relevant academic research and scientific papers

Synthesis of 2H-pyrroles by treatment of pyrrolidines with DDQ

Cheruku, Srinivasa R.,Padmanilayam, Maniyan P.,Vennerstrom, Jonathan L.

, p. 3701 - 3703 (2007/10/03)

A mild and efficient synthesis of 2,2-dialkyl-3,5-diaryl-2H-pyrroles is described. Treatment of 2,2-dialkyl-3,5-diarylpyrrolidines with DDQ in dioxane for 12-24 h at rt afforded the corresponding 2H-pyrroles in 55-81% overall yields.

NEUE WEGE ZU 1H-UND 2H-PYRROLEN

Pfoertner, Karl-Heinz,Foricher, Joseph

, p. 658 - 663 (2007/10/02)

A synthesis of 1H-pyrroles is described starting with pyridine analogues of chalcones and involving the reacxtion of acetic anhydride with 1-pyrroline-1-oxides.Another route leads from 1-pyrrolines to 2H-pyrroles via bromination with N-bromosuccinimide and subsequent dehydrobromination in dimethylformamide.

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