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Cyclopropanecarboxylic acid, 2-benzoyl-, (1R,2R)-rel- is a complex organic compound with the chemical formula C12H12O4. It is a derivative of cyclopropanecarboxylic acid, featuring a benzoyl group attached to the 2-position of the cyclopropane ring. The (1R,2R)-rel- notation indicates the specific relative stereochemistry of the molecule, with the R configuration at both the 1st and 2nd carbon atoms. Cyclopropanecarboxylic acid, 2-benzoyl-, (1R,2R)-rel- is known for its potential applications in pharmaceuticals and chemical research, particularly in the synthesis of various drugs and other bioactive molecules. Its unique structure and properties make it an interesting subject for study in organic chemistry and medicinal chemistry.

1601-82-7

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1601-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1601-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1601-82:
(6*1)+(5*6)+(4*0)+(3*1)+(2*8)+(1*2)=57
57 % 10 = 7
So 1601-82-7 is a valid CAS Registry Number.

1601-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-2-benzoyl-cyclopropanecarboxylic acid

1.2 Other means of identification

Product number -
Other names (+/-)-cis-2-Benzoyl-cyclopropan-carbonsaeure-(1)

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 -
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More Details:1601-82-7 SDS

1601-82-7Relevant academic research and scientific papers

A General Protocol for Radical Anion [3+2] Cycloaddition Enabled by Tandem Lewis Acid Photoredox Catalysis

Amador, Adrian G.,Sherbrook, Evan M.,Lu, Zhan,Yoon, Tehshik P.

supporting information, p. 539 - 547 (2017/10/30)

A method for intermolecular [3+2] cycloaddition between aryl cyclopropyl ketones and alkenes involving the combination of Lewis acid and photoredox catalysis is reported. In contrast to other more common methods for [3+2] cycloaddition, these conditions o

Enantioselective Photocatalytic [3 + 2] Cycloadditions of Aryl Cyclopropyl Ketones

Amador, Adrian G.,Sherbrook, Evan M.,Yoon, Tehshik P.

supporting information, p. 4722 - 4725 (2016/05/10)

Control of stereochemistry in photocycloaddition reactions remains a substantial challenge; almost all successful catalytic examples to date have involved [2 + 2] photocycloadditions of enones. We report a method for the asymmetric [3 + 2] photocycloaddition of aryl cyclopropyl ketones that enables the enantiocontrolled construction of densely substituted cyclopentane structures not synthetically accessible using other catalytic methods. These results show that the dual-catalyst strategy developed in our laboratory broadens synthetic chemists' access to classes of photochemical cycloadditions that have not previously been feasible in enantioselective form.

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