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Methyl (1R,3R)-3-(2-hydroxy-2-methylpropanoyl)-2,2-dimethylcyclopropanecarboxylate is a complex organic compound with the molecular formula C11H18O5. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific (1R,3R) configuration. methyl (1R,3R)-3-(2-hydroxy-2-methylpropanoyl)-2,2-dimethylcyclopropanecarboxylate features a cyclopropane ring, which is a three-membered carbon ring, and a methyl group attached to the carboxylate group. The 2-hydroxy-2-methylpropanoyl moiety indicates the presence of a hydroxyl group and a methyl group on a three-carbon chain that is attached to the cyclopropane ring. This chemical structure is significant in the field of organic chemistry, particularly in the synthesis of certain pharmaceuticals and natural products, due to its unique stereochemistry and ring structure.

2259-16-7

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2259-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2259-16-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,5 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2259-16:
(6*2)+(5*2)+(4*5)+(3*9)+(2*1)+(1*6)=77
77 % 10 = 7
So 2259-16-7 is a valid CAS Registry Number.

2259-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (1R,3R)-3-(2-hydroxy-2-methylpropanoyl)-2,2-dimethylcyclopropane-1-carboxylate

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

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More Details:2259-16-7 SDS

2259-16-7Relevant academic research and scientific papers

Novel synthesis of (d,l) trans-chrysanthemic acid involving a β-diketone fragmentation

Krief, Alain,Jeanmart, Stephane

, p. 6167 - 6168 (2007/10/03)

Methyl (d,l) trans-chrysanthemate as well as its cis-diastereoisomer have been prepared from dimethyl dimedone, one of their isomers, in a few steps and with complete control of the relative stereochemistry.

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