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42019-35-2

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42019-35-2 Usage

Chemical compound

2-[4-(4-Chlorobenzoyl)-3-methylphenoxy]-2-methylpropanoic acid isopropyl ester

Family

Isopropyl esters

Derivative of

2-methylpropanoic acid

Features

4-chlorobenzoyl group attached to a 3-methylphenoxy group

Common uses

Organic synthesis and pharmaceutical research

Applications

Intermediate or building block for the synthesis of various organic compounds

Interest

Unique structure and properties for further exploration and potential applications in different fields

Check Digit Verification of cas no

The CAS Registry Mumber 42019-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,1 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42019-35:
(7*4)+(6*2)+(5*0)+(4*1)+(3*9)+(2*3)+(1*5)=82
82 % 10 = 2
So 42019-35-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H23ClO4/c1-13(2)25-20(24)21(4,5)26-17-10-11-18(14(3)12-17)19(23)15-6-8-16(22)9-7-15/h6-13H,1-5H3

42019-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name propan-2-yl 2-[4-(4-chlorobenzoyl)-3-methylphenoxy]-2-methylpropanoate

1.2 Other means of identification

Product number -
Other names -

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:42019-35-2 SDS

42019-35-2Downstream Products

42019-35-2Relevant articles and documents

Cobalt-catalysed C–H methylation for late-stage drug diversification

Ackermann, Lutz,Friis, Stig D.,Johansson, Magnus J.

, p. 511 - 519 (2020/06/05)

The magic methyl effect is well acknowledged in medicinal chemistry, but despite its significance, accessing such analogues via derivatization at a late stage remains a pivotal challenge. In an effort to mitigate this major limitation, we here present a strategy for the cobalt-catalysed late-stage C–H methylation of structurally complex drug molecules. Enabling broad applicability, the transformation relies on a boron-based methyl source and takes advantage of inherently present functional groups to guide the C–H activation. The relative reactivity observed for distinct classes of functionalities were determined and the sensitivity of the transformation towards a panel of common functional motifs was tested under various reaction conditions. Without the need for prefunctionalization or postdeprotection, a diverse array of marketed drug molecules and natural products could be methylated in a predictable manner. Subsequent physicochemical and biological testing confirmed the magnitude with which this seemingly minor structural change can affect important drug properties. [Figure not available: see fulltext.]

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