(3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine is a unique chemical compound belonging to the class of piperidines, which are organic compounds with a saturated six-member heterocyclic ring containing a nitrogen atom. This specific compound features a 1-Boc-3-fluoro-4-(hydroxyMethyl) substitution pattern on the piperidine ring. The Boc group, a tert-butoxycarbonyl protecting group, is commonly used in organic synthesis to protect amines. The presence of a fluoro and hydroxymethyl substituent on the piperidine ring endows the compound with distinctive physical and chemical properties, making it a promising candidate for pharmaceutical or chemical applications.
882033-94-5
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Basic information
- Product Name: (3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine
- Synonyms: (3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine;(3R,4R)-rel-tert-Butyl 3-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate;(3,4)-Tras-tert-butyl 3-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate;(3,4)-TRANS-TERT-BUTYL 3-FLUORO-4-(HYDROXYMETHYL)PIPERIDINE-1-CARBOXYLATE
- CAS NO:882033-94-5
- Molecular Formula: C11H20FNO3
- Molecular Weight: 233.29
- EINECS: N/A
- Product Categories: N/A
- Mol File: 882033-94-5.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 316.2±27.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.13±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 14.94±0.10(Predicted)
- CAS DataBase Reference: (3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine(CAS DataBase Reference)
- NIST Chemistry Reference: (3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine(882033-94-5)
- EPA Substance Registry System: (3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine(882033-94-5)
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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: 882033-94-5(Hazardous Substances Data)
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882033-94-5 Usage
Uses
Used in Pharmaceutical Industry:(3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine is used as a key intermediate in the synthesis of various pharmaceutical compounds for its unique substitution pattern and protective Boc group. The fluoro and hydroxymethyl substituents on the piperidine ring provide specific properties that can be exploited in the development of new drugs with improved efficacy and selectivity.
Used in Chemical Research:
(3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine is used as a research compound in chemical studies to explore the effects of different substituents on the piperidine ring. (3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine's unique structure allows chemists to investigate its reactivity, stability, and potential applications in various chemical reactions and processes.
Used in Organic Synthesis:
(3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine is used as a building block in organic synthesis for the preparation of more complex molecules. The Boc protecting group can be selectively removed under mild conditions, allowing for further functionalization of the piperidine ring. This makes the compound a versatile starting material for the synthesis of a wide range of organic compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 882033-94-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,0,3 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.Calculate Digit Verification of CAS Registry Number 882033-94:
(8*8)+(7*8)+(6*2)+(5*0)+(4*3)+(3*3)+(2*9)+(1*4)=175
175 % 10 = 5
So 882033-94-5 is a valid CAS Registry Number.
882033-94-5Upstream product
882033-94-5Downstream Products
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(3S,4S)-rel-1-Boc-3-fluoro-4-(hydroxyMethyl)piperidine
