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8-Azabicyclo[3.2.1]oct-3-en-2-one, 8-(4,6-dimethyl-2-pyrimidinyl)-6-phenyl-, endo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62219-60-7

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62219-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62219-60-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,1 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62219-60:
(7*6)+(6*2)+(5*2)+(4*1)+(3*9)+(2*6)+(1*0)=107
107 % 10 = 7
So 62219-60-7 is a valid CAS Registry Number.

62219-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-(4,6-dimethyl-pyrimidin-2-yl)-6-phenyl-8-aza-bicyclo[3.2.1]oct-3-en-2-one

1.2 Other means of identification

Product number -
Other names (1R,5S,6S)-8-(4,6-Dimethyl-pyrimidin-2-yl)-6-phenyl-8-aza-bicyclo[3.2.1]oct-3-en-2-one

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:62219-60-7 SDS

62219-60-7Downstream Products

62219-60-7Relevant academic research and scientific papers

1,3-Dipolar Character of Six-membered Aromatic Rings. Part 48. Novel Conversions of Pyridines to Isoquinolines

Katritzky, Alan R.,Dennis, Nicholas,Dowlatshahi, Hossein A.

, p. 331 - 342 (2007/10/02)

1-Heteroaryl-3-oxidopyridinium dimers with dienamines give cycloadducts which are dehydrogenated to 'mixed dimer' of the corresponding 2-heteroaryl-4-oxidoisoquinolinium with the starting 1-heteroaryl-3-oxidopyridinium.The 'mixed dimer' (21) is also effectively prepared by a two-step sequence of a novel intramolecular oxidation-reduction, followed by oxidation of the resulting alcohol.The 'mixed dimers' undergo reversible thermal dissociation and in one case the corresponding monomers could be trapped as various cycloadducts.

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