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Ethyl 2,3-dihydroxy-3,3-diphenylpropanoate is a chemical compound with the molecular formula C17H18O4. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. ethyl 2,3-dihydroxy-3,3-diphenylpropanoate is an ester derivative of 2,3-dihydroxy-3,3-diphenylpropanoic acid, featuring a central propane chain with two hydroxyl groups at the 2nd and 3rd carbon atoms, and two phenyl rings attached to the 3rd carbon. Ethyl 2,3-dihydroxy-3,3-diphenylpropanoate is primarily used in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity. It is also known for its potential applications in the development of new drugs and as a building block in the creation of complex organic molecules.

5461-98-3

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5461-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5461-98-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5461-98:
(6*5)+(5*4)+(4*6)+(3*1)+(2*9)+(1*8)=103
103 % 10 = 3
So 5461-98-3 is a valid CAS Registry Number.

5461-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,3-dihydroxy-3,3-diphenylpropanoate

1.2 Other means of identification

Product number -
Other names ETHYL 2,3-DIHYDROXY-3,3-DIPHENYL-PROPANOATE

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:5461-98-3 SDS

5461-98-3Relevant academic research and scientific papers

Retropinacol/cross-pinacol coupling reactions - A catalytic access to 1,2-unsymmetrical diols

Scheffler, Ulf,Stoesser, Reinhard,Mahrwald, Rainer

supporting information, p. 2648 - 2652,5 (2012/12/12)

A new concept to access unsymmetrical 1,2-diols with high yields is reported. This new methodology is based on a retropinacol/cross-pinacol coupling process. This transformation is characterized by its operational simplicity and very mild reaction condi tions.

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