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Pyrazolo[1,5-a]pyrimidine, 6-cyclobutyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90253-53-5

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90253-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90253-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,5 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90253-53:
(7*9)+(6*0)+(5*2)+(4*5)+(3*3)+(2*5)+(1*3)=115
115 % 10 = 5
So 90253-53-5 is a valid CAS Registry Number.

90253-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-cyclobutylpyrazolo[1,5-a]pyrimidine

1.2 Other means of identification

Product number -
Other names Pyrazolo[1,5-a]pyrimidine,6-cyclobutyl

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:90253-53-5 SDS

90253-53-5Downstream Products

90253-53-5Relevant academic research and scientific papers

ChemBead Enabled High-Throughput Cross-Electrophile Coupling Reveals a New Complementary Ligand

Aguirre, Ana L.,Loud, Nathan L.,Johnson, Keywan A.,Weix, Daniel J.,Wang, Ying

, p. 12981 - 12986 (2021)

High-throughput experimentation (HTE) methods are central to modern medicinal chemistry. While many HTE approaches to C?N and Csp2?Csp2 bonds are available, options for Csp2?Csp3 bonds are limited. We report here how the adaptation of nickel-catalyzed cross-electrophile coupling of aryl bromides with alkyl halides to HTE is enabled by AbbVie ChemBeads technology. By using this approach, we were able to quickly map out the reactivity space at a global level with a challenging array of 3×222 micromolar reactions. The observed hit rate (56 %) is competitive with other often-used HTE reactions and the results are scalable. A key to this level of success was the finding that bipyridine 6-carboxamidine (BpyCam), a ligand that had not previously been shown to be optimal in any reaction, is as general as the best-known ligands with complementary reactivity. Such “cryptic” catalysts may be common and modern HTE methods should facilitate the process of finding these catalysts.

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