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(Racemic)-methyl 2-aminospiro[3.3]heptane-6-carboxylate hydrochloride is a chemical compound characterized by its unique spirocyclic structure, featuring both an amine and a carboxylate group. The racemic form of (racemic)-methyl 2-aminospiro[3.3]heptane-6-carboxylate hydrochloride consists of equal proportions of its enantiomers, which are mirror-image molecules that may exhibit distinct biological activities. The presence of the hydrochloride salt enhances the solubility and stability of the compound, facilitating its use in laboratory settings. This versatile building block is widely utilized in the synthesis of pharmaceuticals and other organic compounds, with promising applications in drug development and organic chemistry research.

1808249-67-3

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1808249-67-3 Usage

Uses

Used in Pharmaceutical Synthesis:
(Racemic)-methyl 2-aminospiro[3.3]heptane-6-carboxylate hydrochloride serves as a key building block in the synthesis of various pharmaceuticals. Its unique spirocyclic structure and functional groups enable the creation of diverse drug molecules with potential therapeutic applications.
Used in Organic Chemistry Research:
(racemic)-methyl 2-aminospiro[3.3]heptane-6-carboxylate hydrochloride is also employed as a valuable intermediate in organic chemistry research. Its versatile structure and reactivity make it an ideal candidate for exploring novel synthetic pathways and developing new organic compounds with potential applications in various fields.
Used in Drug Development:
The racemic nature of (racemic)-methyl 2-aminospiro[3.3]heptane-6-carboxylate hydrochloride allows for the investigation of the different biological activities of its enantiomers. This can lead to the discovery of more effective and selective drug candidates, as well as a better understanding of the stereoselectivity in drug action.
Used in Enhancing Solubility and Stability:
The hydrochloride salt form of (racemic)-methyl 2-aminospiro[3.3]heptane-6-carboxylate hydrochloride increases its solubility and stability, making it more suitable for use in laboratory settings. This improved solubility can be particularly beneficial in the development of drug formulations and the study of the compound's properties in various solvent systems.

Check Digit Verification of cas no

The CAS Registry Mumber 1808249-67-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,0,8,2,4 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1808249-67:
(9*1)+(8*8)+(7*0)+(6*8)+(5*2)+(4*4)+(3*9)+(2*6)+(1*7)=193
193 % 10 = 3
So 1808249-67-3 is a valid CAS Registry Number.

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