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(R)-Glycidyl-4-nitrobenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118629-64-4

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118629-64-4 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 118629-64-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,2 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 118629-64:
(8*1)+(7*1)+(6*8)+(5*6)+(4*2)+(3*9)+(2*6)+(1*4)=144
144 % 10 = 4
So 118629-64-4 is a valid CAS Registry Number.

118629-64-4Relevant academic research and scientific papers

Initial development of a cytotoxic amino-seco-CBI warhead for delivery by prodrug systems

Twum, Elvis A.,Nathubhai, Amit,Wood, Pauline J.,Lloyd, Matthew D.,Thompson, Andrew S.,Threadgill, Michael D.

, p. 3481 - 3489 (2015)

Abstract Cyclopropabenzaindoles (CBIs) are exquisitely potent cytotoxins which bind and alkylate in the minor groove of DNA. They are not selective for cancer cells, so prodrugs are required. CBIs can be formed at physiological pH by Winstein cyclisation of 1-chloromethyl-3-substituted-5-hydroxy-2,3-dihydrobenzo[e]indoles (5-OH-seco-CBIs). Corresponding 5-NH2-seco-CBIs should also undergo Winstein cyclisation similarly. A key triply orthogonally protected intermediate on the route to 5-NH2-seco-CBIs has been synthesised, via selective monotrifluoroacetylation of naphthalene-1,3-diamine, Boc protection, electrophilic iodination, selective allylation at the trifluoroacetamide and 5-exo radical ring-closure with TEMPO. This intermediate has potential for introduction of peptide prodrug masking units (deactivating the Winstein cyclisation and cytotoxicity), addition of diverse indole-amide side-chains (enhancing non-covalent binding prior to alkylation) and use of different leaving groups (replacing the usual chlorine, allowing tuning of the rate of Winstein cyclisation). This key intermediate was elaborated into a simple model 5-NH2-seco-CBI with a dimethylaminoethoxyindole side-chain. Conversion to a bio-reactive entity and the bioactivity of this system were confirmed through DNA-melting studies (ΔTm = 13°C) and cytotoxicity against LNCaP human prostate cancer cells (IC50 = 18 nM).

PROCESS FOR THE PREPARATION OF CATHEPSIN S INHIBITORS

-

Page/Page column 146-147, (2011/02/24)

Inhibitors of Cathepsin S enzyme and their synthetic processes.

Antagonists of the calcium receptor. 2. Amino alcohol-based parathyroid hormone secretagogues

Marquis, Robert W.,Lago, Amparo M.,Callahan, James F.,Rahman, Attiq,Dong, Xiaoyang,Stroup, George B.,Hoffman, Sandra,Gowen, Maxine,DelMar, Eric G.,Van Wagenen, Bradford C.,Logan, Sarah,Shimizu, Scott,Fox, John,Nemeth, Edward F.,Roethke, Theresa,Smith, Brian R.,Ward, Keith W.,Bhatnagar, Pradip

experimental part, p. 6599 - 6605 (2010/04/03)

When administered as a single agent to rats, the previously reported calcium receptor antagonist 3 elicited a sustained elevation of plasma PTH resulting in no increase in overall bone mineral density. The lack of a bone building effect for analogue 3 was

Chiral glycidyl azides as synthetic intermediates to optically active compounds

-

, (2008/06/13)

Chiral glycidyl azides, such as (2S)-glycidyl azide, are prepared, and they are useful as intermediates to prepare optically active compounds, particularly optically active, anti-bacterial oxazolidinones.

Arenesulfonate Derivatives of Homochiral Glycidol: Versatile Chiral Building Blocks for Organic Synthesis

Klunder, Janice M.,Onami, Tetsuo,Sharpless, K. Barry

, p. 1295 - 1304 (2007/10/02)

The preparation of a series of crystalline arenesulfonate derivatives of enantiomerically enriched glycidol is described.The enhancement of optical purity by recrystallization was particularly successful for two of these derivatives, glycidyl tosylate and glycidyl 3-nitrobenzenesulfonate, which were obtained in 97 percent ee and 99 percent ee, respectively.Very high regioselectivity was observed in the reactions of these compounds with a variety of nucleophiles, including aryl oxides, Et2AlCN, organometallic reagents, and BH3-NaBH4.The application of this methodology to the synthesis of homochiral β-adrenergic blocking agents and homochiral terminal epoxides is discussed.

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