1068-52-6 Usage
Description
Sodium bromoacetate is a chemical compound with the formula CH2BrCOONa. It is a white crystalline solid that is soluble in water and has a salty taste. Sodium bromoacetate is an important raw material and intermediate used in various fields, including organic synthesis, agrochemical, pharmaceutical, and dyestuff industries.
Uses
Used in Organic Synthesis:
Sodium bromoacetate is used as a reagent and intermediate in organic synthesis for the preparation of various organic compounds. It is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and dyes due to its ability to act as a bromine source and a carboxylic acid equivalent.
Used in Agrochemical Industry:
In the agrochemical industry, sodium bromoacetate is used as a precursor for the synthesis of various agrochemicals, such as herbicides and pesticides. Its bromine-containing structure makes it a valuable building block for the development of new and effective agrochemical products.
Used in Pharmaceutical Industry:
Sodium bromoacetate is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to act as a carboxylic acid equivalent and a bromine source allows for the development of new drugs with unique properties and therapeutic applications.
Used in Dye Industry:
In the dye industry, sodium bromoacetate is used as a raw material for the production of various dyes and pigments. Its bromine-containing structure contributes to the color and stability of the dyes, making it an essential component in the dye manufacturing process.
Check Digit Verification of cas no
The CAS Registry Mumber 1068-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1068-52:
(6*1)+(5*0)+(4*6)+(3*8)+(2*5)+(1*2)=66
66 % 10 = 6
So 1068-52-6 is a valid CAS Registry Number.
InChI:InChI=1/C2H3BrO2.Na/c3-1-2(4)5;/h1H2,(H,4,5);/q;+1/p-1
1068-52-6Relevant articles and documents
MACROMOLECULES MODIFIED WITH ELECTROPHILIC GROUPS AND METHODS OF MAKING AND USING THEREOF
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Page/Page column 12, (2010/11/29)
Described herein are macromolecules modified with electrophilic groups and methods of making and using thereof. The preparation of a thiol-reactive, electrophililic derivative of HA in order to prepare “crosslinker-free” hydrogels are described as well as compounds and methods that are capable of coupling two or more molecules, such as macromolecules, under mild conditions. Specifically disclosed is the introduction of reactive bromo- and iodoacetate functionalities at the hydroxyl groups that are abundantly present on the HA polymer. The “crosslinker-free” hydrogels described have numerous applications including, but not limited to, drug delivery, small molecule delivery, wound healing, burn injury healing, tissue regeneration/engineering, cell culturing, and bio-artificial materials.
