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1,2-Oxathiolane,5-ethyl-3-phenyl-,2,2-dioxide,(3R,5R)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

637775-88-3

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637775-88-3 Usage

Physical appearance

White crystalline solid
The compound has a solid form with a white color and a crystalline structure.

Melting point

63-65°C
The temperature range at which the compound transitions from a solid to a liquid state under standard atmospheric pressure.

Optical activity

(3R,5R)-
The compound exhibits chirality, meaning it has a specific three-dimensional arrangement of its atoms, with the (3R,5R) notation indicating the configuration of the chiral centers.

Primary use

Reagent in organic synthesis
The main application of the compound is as a reagent, which is a substance used to promote or facilitate a chemical reaction in the synthesis of other organic compounds.

Industries

Pharmaceutical and chemical
The compound is utilized in both the pharmaceutical and chemical industries, likely due to its reactivity and potential for creating new compounds with various applications.

Potential medical properties

Anti-inflammatory and analgesic
Ethadione has been studied for its possible ability to reduce inflammation and relieve pain, making it a potential candidate for further research and development in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 637775-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,7,7,7 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 637775-88:
(8*6)+(7*3)+(6*7)+(5*7)+(4*7)+(3*5)+(2*8)+(1*8)=213
213 % 10 = 3
So 637775-88-3 is a valid CAS Registry Number.

637775-88-3Upstream product

637775-88-3Relevant academic research and scientific papers

Asymmetric Synthesis of α,γ-Substituted γ-Sultones via Allylation of Chiral Lithiated Sulfonates

Enders, Dieter,Harnying, Wacharee,Vignola, Nicola

, p. 3939 - 3947 (2003)

The first auxiliary controlled asymmetric synthesis of enantiopure α,γ-substituted γ-sultones via α-allylation of lithiated sulfonates by using 1,2:5,6-di-O-isopropylidene-α -D-allofuranose as chiral auxiliary is described. The high asymmetric inductions

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