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52095-58-6

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52095-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52095-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,9 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52095-58:
(7*5)+(6*2)+(5*0)+(4*9)+(3*5)+(2*5)+(1*8)=116
116 % 10 = 6
So 52095-58-6 is a valid CAS Registry Number.

52095-58-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylimidazo[1,5-a]pyridine

1.2 Other means of identification

Product number -
Other names Imidazo[1,5-a]pyridine,1-phenyl

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:52095-58-6 SDS

52095-58-6Relevant articles and documents

Controlled regiodivergent C-H bond activation of imidazo[1,5-a]pyridine via synergistic cooperation between aluminum and nickel

Yu, Ming-Shiuan,Lee, Wei-Chih,Chen, Chih-Hao,Tsai, Fu-Yu,Ong, Tiow-Gan

, p. 4826 - 4829 (2014)

The catalytic method features a cooperative interaction between Ni and Al imparting remote C-H alkenylation at the C5 position of imidazo[1,5-a]pyridine with alkynes at mild conditions. Exclusion of AlMe3 switches the selectivity to the C3 position. Reactions with styrene and other olefinic substrates affording C5-adducts by Ni/Al catalysis are also included.

Isonitrile alkylations: A rapid route to imidazo[1,5-a]pyridines

Li, Yajun,Chao, Allen,Fleming, Fraser F.

supporting information, p. 2111 - 2113 (2016/02/05)

Metalated arylmethylisonitriles readily add to 2-chloropyridines to afford imidazo[1,5-a]pyridines. Analogous additions to imidoyl chlorides and a chloroquinoline provide imidazoles and an imidazo[1,5-a]quinolone which, like imidazo[1,5-a]pyridines, are v

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