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METHYL 3,5-DICHLORO-4-METHOXYBENZOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24295-27-0

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24295-27-0 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 79, p. 1468, 1957 DOI: 10.1021/ja01563a053

Check Digit Verification of cas no

The CAS Registry Mumber 24295-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,9 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24295-27:
(7*2)+(6*4)+(5*2)+(4*9)+(3*5)+(2*2)+(1*7)=110
110 % 10 = 0
So 24295-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Cl2O3/c1-13-8-6(10)3-5(4-7(8)11)9(12)14-2/h3-4H,1-2H3

24295-27-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3,5-dichloro-4-methoxybenzenecarboxylate

1.2 Other means of identification

Product number -
Other names METHYL 3,5-DICHLORO-4-METHOXYBENZOATE

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:24295-27-0 SDS

24295-27-0Relevant academic research and scientific papers

Stereocontrolled total synthesis of (-)-kaitocephalin

Vaswani, Rishi G.,Chamberlin, A. Richard

, p. 1661 - 1681 (2008/09/18)

(Chemical Equation Presented) This paper describes the successful implementation of a stereocontrolled strategy for the total chemical synthesis of the pyrrolidine-based alkaloid (-)-kaitocephalin. This scalable synthetic route profits from the strategic

Induction of apoptosis in cancer cells

-

, (2008/06/13)

The present invention provides compounds that are inducers or inhibitors of apoptosis or apoptosis preceded by cell-cycle arrest. In addition, the present invention provides pharmaceutical compositions and methods for treating mammals with leukemia or other forms of cancer or for treating disease conditions caused by apoptosis of cells.

Synthesis of (1R,2S)-1-(3′-chloro-4′-methoxyphenyl)-1,2- propanediol (trametol) and (1R,2S)-1-(3′,5′-dichloro-4′- methoxyphenyl)-1,2-propanediol, chlorinated fungal metabolites in the natural environment

Kousaka, Takeshi,Mori, Kenji

, p. 697 - 701 (2007/10/03)

(1R,2S)-1-(3′-Chloro-4′-methoxyphenyl)-1,2-propanediol (Trametol, 3), a metabolite of the fungus Trametes sp. IVP-F640 and Bjerkandera sp. BOS55, was synthesized by employing Sharpless asymmetric dihydroxylation as the key step. Similarly, the (1R,2S)-isomer of 1-(3′,5′-dichloro- 4′-methoxyphenyl)-1,2-propanediol (4), another metabolite of Bjerkandera sp. BOS55, was synthesized by asymmetric dihydroxylation.

Synthetic studies towards the synthesis of western and eastern chloropeptin I, II subunits

Roussi, Georges,Gonzalez Zamora, Eduardo,Carbonnelle, Annie-Claude,Beugelmans, Rene

, p. 2041 - 2063 (2007/10/03)

The western subunit (16-membered ring) was synthesized by the intramolecular SNAr reaction while the first 16-membered ring compound was obtained as a model of the eastern subunit via an intramolecular Ni0 mediated coupling reaction.

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