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62289-80-9

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62289-80-9 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 69, p. 2239, 1947 DOI: 10.1021/ja01201a511

Check Digit Verification of cas no

The CAS Registry Mumber 62289-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,8 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62289-80:
(7*6)+(6*2)+(5*2)+(4*8)+(3*9)+(2*8)+(1*0)=139
139 % 10 = 9
So 62289-80-9 is a valid CAS Registry Number.

62289-80-9SDS

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 N-pyridin-2-ylthiophene-2-carboxamide

1.2 Other means of identification

Product number -
Other names Thiophen-2-carbonsaeure-[2]pyridylamid

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:62289-80-9 SDS

62289-80-9Downstream Products

62289-80-9Relevant articles and documents

Copper Catalyzed Oxidative C-C Bond Cleavage of 1,2-Diketones: A Divergent Approach to 1,8-Naphthalimides, Biphenyl-2,2′-dicarboxamides, and N-Heterocyclic Amides

Sakhare, Priyanka R.,Subramanian, Parthasarathi,Kaliappan, Krishna P.

, p. 2112 - 2125 (2019/02/14)

We report here a simple and efficient copper catalyzed oxidative C-C bond cleavage of stable aromatic cyclic-fused and acyclic 1,2-diketones to deliver amides and imides in high yields. This newly developed protocol provides an excellent tool to transform structurally different 1,2-diketones into different products under the same reaction conditions. The key synthetic features of this methodology are the formation of 1,8-naphthalimides and biphenyl-2,2′-dicarboxamide motifs in high yields. The fluorescent studies of 1,8-naphthalimide derivatives were also carried out in order to show the potential application of these scaffolds.

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