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1023648-24-9

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  • Diethyl 2-{2-[4-(3-benzyloxyphenylsulfanyl)-2-chlorophenyl]-ethyl}-2-fluoro-malonate

    Cas No: 1023648-24-9

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1023648-24-9 Usage

Chemical structure

The compound consists of a diethyl ester of malonic acid with substituted phenyl rings.

Substituent groups

It contains a benzyloxy group, a chloro group, and a fluoro group.

Halogenated compound

The presence of the chloro and fluoro groups makes it a halogenated compound.

Lipophilicity

The diethyl ester group makes the compound lipophilic, allowing it to penetrate biological membranes.

Potential applications

The compound may have potential uses in medicinal chemistry, organic synthesis, and material science due to its complex structure and pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1023648-24-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,3,6,4 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1023648-24:
(9*1)+(8*0)+(7*2)+(6*3)+(5*6)+(4*4)+(3*8)+(2*2)+(1*4)=119
119 % 10 = 9
So 1023648-24-9 is a valid CAS Registry Number.

1023648-24-9SDS

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 diethyl 2-[2-[2-chloro-4-(3-phenylmethoxyphenyl)sulfanylphenyl]ethyl]-2-fluoropropanedioate

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:1023648-24-9 SDS

1023648-24-9Downstream Products

1023648-24-9Relevant articles and documents

An efficient total synthesis of a sphingosine-1-phosphate receptor agonist KRP-203

Chino, Masao,Kiuchi, Masatoshi,Adachi, Kunitomo

, p. 3859 - 3866 (2008/09/21)

An efficient total synthesis of the S1P1 agonist, KRP-203, is described. The key step involves the conjugate addition of diethyl acetamidomalonate to a styrene compound to give the core structure of KRP-203. Multigram quantities of the targeted KRP-203, sufficient for several biological studies, were obtained in six steps with an overall yield of 58%.

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