(1S,3S)-3-Aminomethyl-cyclopentanol is a chiral cyclic compound with the molecular formula C6H13NO. It features a five-membered ring that incorporates both a hydroxyl and an amine group, endowing it with unique structural and functional characteristics. (1S,3S)-3-Aminomethyl-cyclopentanol is notable for its chirality, possessing a non-superimposable mirror image, which is significant in the context of stereochemistry and its applications in various fields.
1007306-62-8
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Basic information
- Product Name: (1S,3S)-3-Aminomethyl-cyclopentanol
- Synonyms: (1S,3S)-3-Aminomethyl-cyclopentanol
- CAS NO:1007306-62-8
- Molecular Formula: C6H13NO
- Molecular Weight: 115.17352
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1007306-62-8.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (1S,3S)-3-Aminomethyl-cyclopentanol(CAS DataBase Reference)
- NIST Chemistry Reference: (1S,3S)-3-Aminomethyl-cyclopentanol(1007306-62-8)
- EPA Substance Registry System: (1S,3S)-3-Aminomethyl-cyclopentanol(1007306-62-8)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 1007306-62-8(Hazardous Substances Data)
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1007306-62-8 Usage
Uses
Used in Organic Synthesis:(1S,3S)-3-Aminomethyl-cyclopentanol serves as a versatile building block in organic synthesis, utilized for the construction of more complex molecular architectures. Its presence of both hydroxyl and amine functional groups allows for a wide range of chemical reactions, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (1S,3S)-3-Aminomethyl-cyclopentanol is employed as a key component in the development of new drug candidates. Its unique stereochemistry and the ability to form diverse chemical linkages contribute to its potential in creating novel bioactive compounds with therapeutic applications.
Used in the Development of Bioactive Compounds:
(1S,3S)-3-Aminomethyl-cyclopentanol's structural attributes render it advantageous for the creation of bioactive molecules with specific biological activities. Researchers leverage its reactivity and chirality to design and synthesize compounds that can interact with biological targets, potentially leading to the discovery of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 1007306-62-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,3,0 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.Calculate Digit Verification of CAS Registry Number 1007306-62:
(9*1)+(8*0)+(7*0)+(6*7)+(5*3)+(4*0)+(3*6)+(2*6)+(1*2)=98
98 % 10 = 8
So 1007306-62-8 is a valid CAS Registry Number.
1007306-62-8Upstream product
1007306-62-8Downstream Products
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(1S,3S)-3-Aminomethyl-cyclopentanol
