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4-[(DiMethylaMino)Methyl]-benzoic acid HCl is a chemical compound characterized by a benzoic acid structure with a diethylaminomethyl functional group attached to the fourth carbon atom. It is typically encountered as a hydrochloride salt, offering stability and solubility in aqueous solutions. This versatile compound is utilized as a reagent and intermediate in the synthesis of pharmaceuticals and organic compounds, with potential applications in the development of medications, dyes, and specialty chemicals. Its unique properties and reactivity also make it valuable in research and development settings within the chemical and pharmaceutical industries.

17847-26-6

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17847-26-6 Usage

Uses

Used in Pharmaceutical Synthesis:
4-[(DiMethylaMino)Methyl]-benzoic acid HCl is used as a reagent and intermediate for the synthesis of various pharmaceuticals, contributing to the development of new medications due to its unique chemical structure and reactivity.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 4-[(DiMethylaMino)Methyl]-benzoic acid HCl is employed as a reagent and intermediate, facilitating the creation of a range of organic compounds for diverse applications.
Used in Dye Production:
4-[(DiMethylaMino)Methyl]-benzoic acid HCl is used as a component in the production of dyes, leveraging its chemical properties to contribute to the coloration and stability of these products.
Used in Specialty Chemicals Development:
4-[(DiMethylaMino)Methyl]-benzoic acid HCl is utilized in the development of specialty chemicals, where its specific attributes can be harnessed for targeted applications in various industries.
Used in Research and Development Laboratories:
4-[(DiMethylaMino)Methyl]-benzoic acid HCl is used in research settings for its unique properties and reactivity, aiding in the advancement of scientific knowledge and the discovery of new chemical processes or products.
Used in Chemical and Pharmaceutical Industries:
In these industries, 4-[(DiMethylaMino)Methyl]-benzoic acid HCl is used for its stability and solubility in aqueous solutions, making it suitable for a wide range of applications, from the synthesis of new compounds to the improvement of existing processes.

Check Digit Verification of cas no

The CAS Registry Mumber 17847-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,4 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17847-26:
(7*1)+(6*7)+(5*8)+(4*4)+(3*7)+(2*2)+(1*6)=136
136 % 10 = 6
So 17847-26-6 is a valid CAS Registry Number.

17847-26-6Downstream Products

17847-26-6Relevant academic research and scientific papers

Reconfiguration of π-conjugated superstructures enabled by redox-assisted assembly

Liu, Kaixuan,Mukhopadhyay, Arindam,Ashcraft, Adam,Liu, Chuan,Levy, Adam,Blackwelder, Patricia,Olivier, Jean-Hubert

, p. 5603 - 5606 (2019)

We show that n-doping supramolecular assemblies built from perylene diimide units provides a means to modulate the structure-function properties of these materials. In addition to highlighting the design principles, a combination of spectroscopic and micr

Synthesis and biological evaluation of Matijing-Su derivatives as potent anti-HBV agents

Qiu, Jingying,Xu, Bixue,Huang, Zhengming,Pan, Weidong,Cao, Peixue,Liu, Changxiao,Hao, Xiaojiang,Song, Baoan,Liang, Guangyi

experimental part, p. 5352 - 5360 (2011/10/12)

A series of Matijing-Su (MTS, N-(N-benzoyl-l-phenylalanyl)-O-acetyl-l- phenylalanol) derivatives were synthesized and evaluated for their anti-hepatitis B virus (HBV) activity in 2.2.15 cells. The IC50 of compounds 14a (0.71 μM), 13c (2.85 μM), 13b (4.37 μM), etc. and the selective index of 13g (161.01), 13c (90.45), 13a (85.09) etc. of the inhibition on the replication of HBV DNA were better than those of the positive control lamivudine (IC50: 82.42 μM, SI: 41.59). Compounds 13o, 13p, and 16a also exhibited significant anti-HBV activity.

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