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1015484-23-7

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1015484-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1015484-23-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,5,4,8 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1015484-23:
(9*1)+(8*0)+(7*1)+(6*5)+(5*4)+(4*8)+(3*4)+(2*2)+(1*3)=117
117 % 10 = 7
So 1015484-23-7 is a valid CAS Registry Number.

1015484-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium N-methyl-N-(trifluoroboratomethyl)cyclohexylamine

1.2 Other means of identification

Product number -
Other names POTASSIUM N-CYCLOHEXYL-N-METHYL-AMINOMETHYLTRIFLUOROBORATE

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:1015484-23-7 SDS

1015484-23-7Relevant articles and documents

Synthesis of Arylethylamines via C(sp3)-C(sp3) Palladium-Catalyzed Cross-Coupling

Lippa, Rhys A.,Battersby, David J.,Murphy, John A.,Barrett, Tim N.

, p. 3583 - 3604 (2021/02/27)

Substituted arylethylamines represent a key structural motif in natural, pharmaceutical, and agrochemical compounds. Access to such scaffolds has been the subject of long-standing synthetic interest. Herein, we report the synthesis of such scaffolds via a palladium-catalyzed C(sp3)-C(sp3) coupling between (chloromethyl)aryls and air-/moisture-stable N,N-dialkylaminomethyltrifluoroborate salts. Rapid hit identification was achieved using microscale high-throughput experimentation and was followed by millimolar-scale reaction parameter optimization. A range of structurally and electronically varied arylethylamine products were obtained in moderate to excellent yields (27-96%, >60 examples). The reaction mechanism is proposed to proceed via formation of a trialkylbenzylammonium species prior to oxidative addition.

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