759-97-7 Usage
Uses
Used in Pharmaceutical Industry:
2-BROMO-1,1,3-TRIMETHOXYPROPANE 95 is used as an intermediate in the production of various pharmaceuticals. It plays a crucial role in the synthesis of active pharmaceutical ingredients, contributing to the development of new and effective medications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-BROMO-1,1,3-TRIMETHOXYPROPANE 95 is utilized as an intermediate for the synthesis of various agrochemicals. Its use in this sector helps in the development of pesticides, herbicides, and other agricultural chemicals that are essential for crop protection and increased yield.
Used as a Solvent in Organic Synthesis:
2-BROMO-1,1,3-TRIMETHOXYPROPANE 95 is used as a solvent in organic synthesis due to its ability to dissolve a wide range of organic compounds. Its solubility properties make it a valuable component in various chemical reactions, facilitating the formation of desired products.
Used as a Reagent in Organic Synthesis:
As a reagent, 2-BROMO-1,1,3-TRIMETHOXYPROPANE 95 is involved in numerous organic reactions, often acting as a reactant in the synthesis of complex organic molecules. Its reactivity allows it to participate in various chemical transformations, contributing to the formation of target compounds.
Used in the Preparation of Various Compounds:
2-BROMO-1,1,3-TRIMETHOXYPROPANE 95 is also used as a reactant in the preparation of different compounds, including specialty chemicals, fine chemicals, and other organic substances. Its versatility in reacting with various substrates makes it a valuable component in the synthesis of a wide range of products.
Check Digit Verification of cas no
The CAS Registry Mumber 759-97-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 759-97:
(5*7)+(4*5)+(3*9)+(2*9)+(1*7)=107
107 % 10 = 7
So 759-97-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H13BrO3/c1-8-4-5(7)6(9-2)10-3/h5-6H,4H2,1-3H3
759-97-7Relevant academic research and scientific papers
Claisen Orthoester Rearrangement in the Direct Preparation of Z-Isositsirikine and Z-Geissoschizine Derivatives Possessing the Right Oxidation State at C-17
Lounasmaa, Mauri,Hanhinen, Pirjo,Jokela, Reija
, p. 8623 - 8648 (2007/10/02)
The Claisen orthoester rearrangement utilizing allylic alcohol 1 (or 2) and trimethyl 3-methoxyorthopropionate 13a leads to Z-isositsirikine derivatives 21a-22a (or 23a-24a) possessing one RO-function at C-17.In the cases of trialkyl 3,3-dialkoxyorthopropionates , the intermediate ketene acetals 25a,b do not rearrange according to the Claisen mechanism to form compounds 26a,b and/or possessing two two RO-functions at C-17.Syntheses of the intermediate orthoesters, trimethyl 3-methoxyorthopropionate 13a, trimethyl 3,3-dimethoxyorthopropionate 14a, trimethyl trans-3-methoxyorthoacrylate 20c, and triethyl 3,3-diethoxyorthopropionate 14b are described.
