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Ethanol, 2-(methylpropylamino)-, also known as 2-(2-methylpropylamino)ethanol or tert-amyl alcohol, is an organic compound with the chemical formula C7H17NO. It is a colorless, viscous liquid with a mild, amine-like odor. Ethanol, 2-(methylpropylamino)- is a derivative of ethanol, where one of the hydrogen atoms is replaced by a 2-methylpropylamine group. It is used as a solvent, a chemical intermediate, and in the synthesis of various pharmaceuticals and agrochemicals. Due to its potential health risks, including irritation to the eyes, skin, and respiratory system, as well as its classification as a hazardous substance, it is important to handle this chemical with care and in accordance with safety regulations.

2893-45-0

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2893-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2893-45-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2893-45:
(6*2)+(5*8)+(4*9)+(3*3)+(2*4)+(1*5)=110
110 % 10 = 0
So 2893-45-0 is a valid CAS Registry Number.

2893-45-0Downstream Products

2893-45-0Relevant academic research and scientific papers

pH-Sensitive Polycations for siRNA Delivery: Effect of Asymmetric Structures of Tertiary Amine Groups

Yang, Qinping,Dong, Yanliang,Wang, Xuanyu,Lin, Zhihao,Yan, Mingyu,Wang, Weiwei,Dong, Anjie,Zhang, Jianhua,Huang, Pingsheng,Wang, Changrong

, (2021/03/31)

pH-sensitive polyelectrolytes provide enormous opportunity for siRNA delivery. Especially, their tertiary amine structures can not only bind genes but also act as pH-sensitive hydrophobic structure to control genes release. However, the influence of molecular structures on siRNA delivery still remains elusive, especially for the asymmetric alkyl substituents of the tertiary amine groups. Herein, a library of N-methyl-N-alkyl aminoethyl methacrylate monomers (MsAM) with asymmetric alkyl substituents on the tertiary amine group is synthesized and used to prepare a series of tri-block polycationic copolymers poly(aminoethyl methacrylate)-block-poly (N-methyl-N-alkyl aminoethyl methacrylate)-block-poly(ethylene glycol methacrylate) (PAMA-PMsMA-PEG). And the properties of these polycations and their self-assembled micelles are characterized, including molecular structure, proton buffering capacity, pH-sensitivity, size, and zeta potential. With the length increase of one alkyl substituent, the proton buffering capacity of both monomers and polycations is demonstrated to be narrowed down. The siRNA delivery efficiency and cytotoxicity of these micelles are also evaluated on HepG2 cells. In particular, poly(aminoethyl methacrylate)-block-poly(N-methyl-N-ethyl aminoethyl methacrylate)-block-poly(ethylene glycol methacrylate) (PAMA-PMEMA-PEG) elicited the best luciferase knockdown efficiency and low cytotoxicity. Besides, PAMA-PMEMA-PEG/siRRM2 also induced significant anti-tumor activity in vitro. These results indicated PAMA-PMEMA-PEG has potential for further use in the design of gene vehicles with the improved efficiency of siRNA delivery.

NOVEL THIENOPYRIMIDINE DERIVATIVES OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF, PROCESS FOR THE PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

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Page/Page column 106, (2010/11/28)

The present invention relates to a novel thienopyrimidine derivative having an excellent anti? inflammatory and anti-cancer activity, or a pharmaceutically acceptable salt thereof, a process for the preparation thereof and a pharmaceutical composition comprising the same. The compound according to the present invention strongly inhibits IKB kinase-β (IKK-β) involved in the activation of a transcriptional factor, NF-κB, which is associated with inducing various immune and inflammatory diseases, whereby a composition comprising the compound is a useful therapeutic agent against inflammatory diseases, in particular, arthritis and cancer.

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