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tert-butyl (4-(2-hydroxyethoxy)phenyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

201741-15-3

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201741-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201741-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,7,4 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 201741-15:
(8*2)+(7*0)+(6*1)+(5*7)+(4*4)+(3*1)+(2*1)+(1*5)=83
83 % 10 = 3
So 201741-15-3 is a valid CAS Registry Number.

201741-15-3Downstream Products

201741-15-3Relevant academic research and scientific papers

Bispecific Estrogen Receptor α Degraders Incorporating Novel Binders Identified Using DNA-Encoded Chemical Library Screening

Disch, Jeremy S.,Duffy, Jennifer M.,Lee, Esther C. Y.,Gikunju, Diana,Chan, Betty,Levin, Benjamin,Monteiro, Michael I.,Talcott, Sarah A.,Lau, Anthony C.,Zhou, Fei,Kozhushnyan, Anton,Westlund, Neil E.,Mullins, Patrick B.,Yu, Yan,Von Rechenberg, Moritz,Zhang, Junyi,Arnautova, Yelena A.,Liu, Yanbin,Zhang, Ying,McRiner, Andrew J.,Keefe, Anthony D.,Kohlmann, Anna,Clark, Matthew A.,Cuozzo, John W.,Huguet, Christelle,Arora, Shilpi

, p. 5049 - 5066 (2021/05/06)

Bispecific degraders (PROTACs) of ERα are expected to be advantageous over current inhibitors of ERα signaling (aromatase inhibitors/SERMs/SERDs) used to treat ER+ breast cancer. Information from DNA-encoded chemical library (DECL) screening provides a me

Iron(III)triflate as a highly efficient, recyclable and green catalyst for the N-Boc protection of amines

Feng, Chengliang,Chu, Ningning,Zhang, Shuguang,Cai, Jin,Chen, Junqing,Hu, Huayou,Ji, Min

, p. 757 - 760 (2014/01/23)

Iron (III) triflate was used as an efficient catalyst for N-t-butoxycarbonylation of amines with di-t-butyl dicarbonate under solvent-free conditions at room temperature. Various aliphatic, aromatic, heterocyclic amines and aminols were protected as their corresponding mono-carbamates in excellent yields and short reaction times. Only two of the 23 monocarbamates were new. No competitive side reactions such as isocyanate, urea, nor N,N-di-Boc formation were observed. The reported method is mild and has the advantages of low cost, chemoselectivity and, because no solvent is used and the catalyst can be recycled, it is classifiable as a green procedure.

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