(1S,3R)-3-aminocyclohexyl acetate, also known as L-tartaric acid 3-aminocyclohexyl ester, is a chiral compound that features a cyclohexane ring with an amino group attached to the third carbon and an acetate group attached to the first carbon. (1S,3R)-3-aminocyclohexyl acetate possesses distinct S and R configurations, which contribute to its unique properties and applications in various fields.
1237714-87-2
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Basic information
- Product Name: (1S,3R)-3-aminocyclohexyl acetate
- Synonyms: (1S,3R)-3-aminocyclohexyl acetate
- CAS NO:1237714-87-2
- Molecular Formula:
- Molecular Weight: 157.213
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (1S,3R)-3-aminocyclohexyl acetate(CAS DataBase Reference)
- NIST Chemistry Reference: (1S,3R)-3-aminocyclohexyl acetate(1237714-87-2)
- EPA Substance Registry System: (1S,3R)-3-aminocyclohexyl acetate(1237714-87-2)
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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: 1237714-87-2(Hazardous Substances Data)
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1237714-87-2 Usage
Uses
Used in Pharmaceutical Synthesis:(1S,3R)-3-aminocyclohexyl acetate is utilized as a chiral resolving agent in the synthesis of pharmaceuticals and other organic compounds. Its specific stereochemistry allows for the creation of enantiomerically pure products, which is crucial for the development of effective and safe medications.
Used in Organic Synthesis:
(1S,3R)-3-aminocyclohexyl acetate serves as a precursor for the preparation of other chiral compounds, which are essential in various chemical processes and industries. Its unique structure and chiral properties make it a valuable building block for the synthesis of complex organic molecules.
Used as a Catalyst in Organic Reactions:
(1S,3R)-3-aminocyclohexyl acetate is also employed as a catalyst in a range of organic reactions. Its ability to selectively influence the course of chemical reactions and enhance the yield of desired products makes it an important tool in organic chemistry and research.
Used in Chiral Chemical Research:
Due to its distinct S and R configurations, (1S,3R)-3-aminocyclohexyl acetate is a valuable compound for studying the effects of chirality on chemical reactions and the properties of molecules. This research can lead to a better understanding of the role of chirality in various chemical and biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1237714-87-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,7,7,1 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.Calculate Digit Verification of CAS Registry Number 1237714-87:
(9*1)+(8*2)+(7*3)+(6*7)+(5*7)+(4*1)+(3*4)+(2*8)+(1*7)=162
162 % 10 = 2
So 1237714-87-2 is a valid CAS Registry Number.
1237714-87-2Upstream product
1237714-87-2Downstream Products
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(1S,3R)-3-aminocyclohexyl acetate
