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2-Naphthalenecarboxylic acid, 1,3-dihydroxy-, methyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

436864-84-5

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436864-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 436864-84-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,8,6 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 436864-84:
(8*4)+(7*3)+(6*6)+(5*8)+(4*6)+(3*4)+(2*8)+(1*4)=185
185 % 10 = 5
So 436864-84-5 is a valid CAS Registry Number.

436864-84-5Downstream Products

436864-84-5Relevant articles and documents

Benzannulation of arynes with dimethylacetonedicarboxylates via an insertion-fragmentation-Dieckman-aromatization cascade: Expeditious entry to naphthoresorcinols and binaphthoresorcinols

Singh, Shweta,Samineni, Ramesh,Pabbaraja, Srihari,Mehta, Goverdhan

, p. 2923 - 2932 (2019/04/30)

Aryne insertions into 1,3,5-tricarbonyl bearing dimethylacetonedicarboxylate (DMAD) proceeds through a 4-step cascade process to eventuate in a versatile one pot synthesis of functionally embellished naphthoresorcinols. Functional group amplifications and

Transition-Metal-Free Benzannulation of Tricarbonyl Derivatives with Arynes: Access to 1,3-Dinaphthol Precursors for the Synthesis of Rhodamine Dye Analogues

Ghotekar, Ganesh S.,Shaikh, Aslam C.,Muthukrishnan

, p. 2269 - 2276 (2019/05/16)

Herein, we report a transition-metal-free annulation reaction of benzynes and 1,3-oxopentanedioate for the synthesis of highly functionalized naphthalene derivatives for the first time. Additionally, the representative naphthalene derivatives have been successfully transformed into the new series of rhodamine dye analogues.

Direct displacement of alkoxy groups of vinylogous esters by grignard reagents

Brockway, Anthony J.,González-López, Marcos,Fettinger, James C.,Shaw, Jared T.

supporting information; experimental part, p. 3515 - 3518 (2011/06/24)

The direct displacement of alkoxy groups from the β position of aromatic and unsaturated esters and ketones is described. The reaction is chemo- and regioselective, displaying wide substrate scope.

Selective protein tyrosine phosphatatase inhibitors

-

, (2008/06/13)

Compounds of formula (I) or therapeutically acceptable salts thereof, are selective protein tyrosine kinase-B (PTP1B) inhibitors. Preparation of the compounds, compositions containing the compounds, and treatment of disorders using the compounds are disclosed.

Selective protein tyrosine phosphatatase inhibitors

-

, (2008/06/13)

Compounds of formula (I) or therapeutically acceptable salts thereof, are selective protein tyrosine kinase-B (PTP1B) inhibitors. Preparation of the compounds, compositions containing the compounds, and treatment of disorders using the compounds are disclosed.

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