181486-37-3 Usage
Description
4-ACETYL-3,5-DIOXO-1-METHYLCYCLOHEXANECARBOXYLIC ACID is a versatile chemical compound belonging to the class of acetylated cyclohexanecarboxylic acids. It features a cyclohexane ring with four substituents, including an acetyl group and two carbonyl groups, which contribute to its chemical reactivity and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
4-ACETYL-3,5-DIOXO-1-METHYLCYCLOHEXANECARBOXYLIC ACID is used as an intermediate in the synthesis of pharmaceuticals for its ability to participate in various chemical reactions, facilitating the creation of diverse medicinal compounds.
Used in Organic Chemistry:
In the field of organic chemistry, 4-ACETYL-3,5-DIOXO-1-METHYLCYCLOHEXANECARBOXYLIC ACID serves as a key building block for the development of complex organic molecules, leveraging its structural features and functional groups to form new compounds with specific properties.
Used in Chemical Research:
4-ACETYL-3,5-DIOXO-1-METHYLCYCLOHEXANECARBOXYLIC ACID is utilized in chemical research to explore its reactivity and potential applications, providing insights into the synthesis of novel compounds and understanding the underlying chemical mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 181486-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,4,8 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 181486-37:
(8*1)+(7*8)+(6*1)+(5*4)+(4*8)+(3*6)+(2*3)+(1*7)=153
153 % 10 = 3
So 181486-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O5/c1-5(11)8-6(12)3-10(2,9(14)15)4-7(8)13/h11H,3-4H2,1-2H3,(H,14,15)/b8-5-
181486-37-3Relevant articles and documents
A new linker for primary amines applicable to combinatorial approaches
Bannwarth, Willi,Huebscher, Josef,Barner, Richard
, p. 1525 - 1528 (2007/10/03)
We describe a new linker molecule (ADCC-linker) for the attachment of primary amines to solid support. The linker is stable towards acidic conditions (eg. TFA) basic conditions (eg. piperidine, DBU) as well as towards uronium type coupling reagents. The amine can be quantitatively released from the support using a 2% hydrazine in DMF solution.