67638-54-4 Usage
Uses
Used in Organic Synthesis:
Bromoacetic acid 1,4-butanediyl ester is used as a key intermediate in the synthesis of various organic compounds, facilitating the formation of complex molecules and contributing to the development of new chemical entities.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Bromoacetic acid 1,4-butanediyl ester is used as a precursor in the synthesis of drugs, playing a crucial role in the creation of medicinal compounds that address various health conditions.
Used in Agrochemicals:
Bromoacetic acid 1,4-butanediyl ester is employed in the production of agrochemicals, contributing to the development of pesticides and other agricultural chemicals that enhance crop protection and yield.
Used in Functional Materials:
This ester is utilized in the synthesis of functional materials with specific properties, such as conductivity, magnetism, or catalytic activity, which are essential in various industrial applications.
Used as a Solvent:
Bromoacetic acid 1,4-butanediyl ester is used as a solvent in certain chemical processes, providing a medium for reactions to occur and facilitating the dissolution of various substances.
Used as a Reagent in Chemical Reactions:
In esterification, acylation, and alkylation reactions, Bromoacetic acid 1,4-butanediyl ester serves as a reagent, enabling the transformation of starting materials into desired products and advancing the progress of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 67638-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,3 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67638-54:
(7*6)+(6*7)+(5*6)+(4*3)+(3*8)+(2*5)+(1*4)=164
164 % 10 = 4
So 67638-54-4 is a valid CAS Registry Number.
67638-54-4Relevant academic research and scientific papers
Holewinski, Ronald J.,Creighton, Donald J.
, p. 3301 - 3308 (2014)
The glyoxalase pathway is responsible for conversion of cytotoxic methylglyoxal (MG) to d-lactate. MG toxicity arises from its ability to form advanced glycation end products (AGEs) on proteins, lipids and DNA. Studies have shown that inhibitors of glyoxa
Studies on synthesis, characterization, micellar features, and solubilization of four novel cationic gemini surfactants
Bilgen, Sel?uk,Sarikaya, Ikbal,ünver, Yasemin,Akba?, Halide
, p. 1522 - 1532 (2021/04/02)
Four novel cationic gemini surfactants with the same hydrocarbon chain lengths but different spacers have been investigated in this article. After these cationic gemini surfactants have been synthesized, their structures have been characterized by appropr
Synthesizing method of imidazole type Gemini surfactant
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Paragraph 0018, (2016/10/09)
The invention discloses a synthesizing method of imidazole type Gemini surfactant. The synthesizing method is characterized in that N-alkyl imidazole is synthesized by using imidazole and alkyl bromide, reaction temperature is 25 DEG C, reaction time is 8 hours, and the yield is about 70%; bromoacetic acid 1, 4-butanediyl ester is synthesized by using bromoacetic acid and dihydric alcohol, reaction temperature is 125 DEG C, and reaction time is 24 hours; the final product is synthesized by using the N-alkyl imidazole and the bromoacetic acid 1, 4-butanediyl ester, reaction temperature is 85 DEG C, reaction time is 36 hours, and yield is about 85%. The synthesizing path is shown as follows, wherein n=2, 4, 6.
