54149-17-6 Usage
Description
1-Bromo-2-(2-methoxyethoxy)ethane, also known as 1-Bromo-2-methoxyethyl ether, is an organic compound that serves as a crucial intermediate in various chemical reactions. It is a clear colorless to pale yellow liquid with unique chemical properties that make it valuable in a range of applications.
Uses
1-Bromo-2-(2-methoxyethoxy)ethane is used as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and dyestuffs. Its versatility in chemical reactions and compatibility with a wide range of substances make it an essential component in these industries.
Used in Pharmaceutical Industry:
1-Bromo-2-(2-methoxyethoxy)ethane is used as a building block for the synthesis of various pharmaceutical compounds. Its ability to participate in a range of chemical reactions allows for the creation of diverse drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-Bromo-2-(2-methoxyethoxy)ethane is used as a starting material for the development of new pesticides and other agricultural chemicals. Its reactivity and stability contribute to the production of effective and environmentally friendly products.
Used in Dye Industry:
1-Bromo-2-(2-methoxyethoxy)ethane is used as an intermediate in the production of various dyes and pigments. Its chemical properties enable the creation of a wide array of colorants for use in textiles, plastics, and other industries.
Used in Organic Synthesis:
1-Bromo-2-(2-methoxyethoxy)ethane is used as a versatile reagent in organic synthesis, allowing for the formation of a variety of complex molecules. Its unique properties make it a valuable tool in the development of new compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 54149-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,4 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54149-17:
(7*5)+(6*4)+(5*1)+(4*4)+(3*9)+(2*1)+(1*7)=116
116 % 10 = 6
So 54149-17-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H11BrO2/c1-7-4-5-8-3-2-6/h2-5H2,1H3
54149-17-6Relevant articles and documents
Thiourea-Mediated Halogenation of Alcohols
Mohite, Amar R.,Phatake, Ravindra S.,Dubey, Pooja,Agbaria, Mohamed,Shames, Alexander I.,Lemcoff, N. Gabriel,Reany, Ofer
, p. 12901 - 12911 (2020/11/26)
The halogenation of alcohols under mild conditions expedited by the presence of substoichiometric amounts of thiourea additives is presented. The amount of thiourea added dictates the pathway of the reaction, which may diverge from the desired halogenation reaction toward oxidation of the alcohol, in the absence of thiourea, or toward starting material recovery when excess thiourea is used. Both bromination and chlorination were highly efficient for primary, secondary, tertiary, and benzyl alcohols and tolerate a broad range of functional groups. Detailed electron paramagnetic resonance (EPR) studies, isotopic labeling, and other control experiments suggest a radical-based mechanism. The fact that the reaction is carried out at ambient conditions, uses ubiquitous and inexpensive reagents, boasts a wide scope, and can be made highly atom economic, makes this new methodology a very appealing option for this archetypical organic reaction.
THIAZOLIDINONE COMPOUNDS AND USE THEREOF
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Paragraph 1254-1255, (2017/09/21)
A pharmaceutical composition containing a compound of Formula (I) for treating an opioid receptor-associated condition. Also disclosed is a method for treating an opioid receptor-associated condition using such a compound. Further disclosed are two sets of thiazolidinone compounds of formula (I): (i) compounds each having an enantiomeric excess greater than 90% and (ii) compounds each being substituted with deuterium.
SYNTHESIS OF DIFUNCTIONAL OXYETHYLENE-BASED COMPOUNDS
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Page/Page column 2-3, (2009/07/25)
A method of reacting a toluenesulfonyl-terminated polyoxyethylene compound having the formula CH3—C6H4—SO2—(O—CH2—CH2)n—O—R1 with an ammonium salt having the formula NR24X to form a compound having the formula X—CH2—CH2—(O—CH2—CH2)n-1—R3. The value n is a positive integer. X is a halogen, cyanide, cyanate, thiocyanate, or azide. R1 is a terminating group. Each R2 is hydrogen or an alkyl group. —R3 is —O—R1 or —X.
