349494-36-6 Usage
Description
(1S,3R,4R)-3,4-dibromocyclohexanecarboxylic acid is a chiral chemical compound with the molecular formula C8H11Br2O2. It features a cyclohexane ring with two bromine atoms and a carboxylic acid group, making it a versatile compound for various chemical reactions and transformations. (1S,3R,4R)-3,4-dibromocyclohexanecarboxylic acid is commonly used in organic synthesis and medicinal chemistry, and has potential applications in pharmaceuticals and agrochemicals due to its ability to act as a building block for more complex molecules. However, it is important to handle this compound with care, as it is a corrosive and toxic substance.
Uses
Used in Organic Synthesis:
(1S,3R,4R)-3,4-dibromocyclohexanecarboxylic acid is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure allows for various chemical reactions and transformations, making it a valuable compound in the synthesis of pharmaceuticals and agrochemicals.
Used in Medicinal Chemistry:
In medicinal chemistry, (1S,3R,4R)-3,4-dibromocyclohexanecarboxylic acid is used as a key intermediate in the development of new drugs. Its chiral nature and functional groups enable the creation of enantiomerically pure compounds, which are essential for the design of effective and selective pharmaceuticals.
Used in Pharmaceutical Industry:
(1S,3R,4R)-3,4-dibromocyclohexanecarboxylic acid is used as a starting material in the pharmaceutical industry for the synthesis of various drug candidates. Its ability to act as a building block for more complex molecules makes it a valuable asset in the development of new therapeutic agents.
Used in Agrochemical Industry:
(1S,3R,4R)-3,4-dibromocyclohexanecarboxylic acid is also used in the agrochemical industry for the synthesis of pesticides and other agrochemical products. Its versatility in chemical reactions allows for the development of new and improved products for agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 349494-36-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,4,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 349494-36:
(8*3)+(7*4)+(6*9)+(5*4)+(4*9)+(3*4)+(2*3)+(1*6)=186
186 % 10 = 6
So 349494-36-6 is a valid CAS Registry Number.
349494-36-6Relevant articles and documents
Stereoisomers of 4-amino-3-hydroxy-1-cyclohexanecarboxylic acid and 4-amino-3-oxo-1-cyclohexanecarboxylic acid as mimetics of a twisted cis-amide bond
Krajewski, Krzysztof,Ciunik, Zbigniew,Siemion, Ignacy Z.
, p. 455 - 462 (2001)
Stereoselective synthesis of the title compounds was performed. The relative configuration of methyl t-4-(tert-butoxycarbonylamino)-c-3-hydroxy-r-1-cyclohexanecarboxylate and methyl trans-4-(tert-butoxycarbonylamino)-3-oxo-r-1-cyclohexanecarboxylate was c
