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Carbamic acid, [2-[4-(phenylmethoxy)phenoxy]ethyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

802971-61-5

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802971-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 802971-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,2,9,7 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 802971-61:
(8*8)+(7*0)+(6*2)+(5*9)+(4*7)+(3*1)+(2*6)+(1*1)=165
165 % 10 = 5
So 802971-61-5 is a valid CAS Registry Number.

802971-61-5Relevant academic research and scientific papers

Anion-templated assembly of a [2]catenane

Sambrook, Mark R.,Beer, Paul D.,Wisner, James A.,Paul, Rowena L.,Cowley, Andrew R.

, p. 15364 - 15365 (2004)

The first example of a [2]catenane structure to be synthesized using anion templation is described. The nature of the anion template is demonstrated to be crucial to the assembly process, with only chloride anion producing the [2]catenane in acceptable yi

Design and synthesis of novel benzothiophene analogs as selective estrogen receptor covalent antagonists against breast cancer

Bai, Chengfeng,Ren, Shengnan,Wu, Shuangjie,Zhu, Meiqi,Luo, Guoshun,Xiang, Hua

, (2021/05/27)

Endocrine therapy (ET) has benefited patients with estrogen receptor alpha (ERα) positive breast cancer for decades. Selective estrogen receptor modulator (SERM) such as Tamoxifen represents the clinical standard of care (SoC). Despite the therapeutic importance of current SoC agents, 30–50% of prolonged treatment patients inevitably generated resistant tumor cells, usually eventually suffered tumor relapse and developed into metastatic breast cancer (MBC), which was the leading cause of female cancer-related mortality. Among these, most resistant tumors remained dependent on ERα signaling, which reignited the need for the next generation of ERα related agents. We hypothesized that selective estrogen receptor covalent antagonists targeting ERα would provide a therapeutic alternative. In the current work, series of novel benzothiophene hybrids bearing electrophile moieties were synthesized and biologically evaluated. The representative analogue 15c exhibited potent anti-proliferative effect in MCF-7 cell lines in vitro, and further mechanism studies confirmed the necessity of covalent bonding. More importantly, 15c could attenuate the expression of TFF-1, GREB-1 and downregulate the levels of cellular ERα protein.

Chloride-Anion-Templated Synthesis of a Strapped-Porphyrin-Containing Catenane Host System

Brown, Asha,Langton, Matthew J.,Kilah, Nathan L.,Thompson, Amber L.,Beer, Paul D.

supporting information, p. 17664 - 17675 (2015/12/08)

The synthesis, structure and anion-recognition properties of a new strapped-porphyrin-containing [2]catenane anion host system are described. The assembly of the catenane is directed by discrete chloride anion templation acting in synergy with secondary aromatic donor-acceptor and coordinative pyridine-zinc interactions. The [2]catenane incorporates a three-dimensional, hydrogen-bond-donating anion-binding pocket; solid-state structural analysis of the catenane-chloride complex reveals that the chloride anion is encapsulated within the catenane's interlocked binding cavity through six convergent CH...Cl and NH...Cl hydrogen-bonding interactions and solution-phase 1H NMR titration experiments demonstrate that this complementary hydrogen-bonding arrangement facilitates the selective recognition of chloride over larger halide anions in DMSO solution.

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