1-Boc-4-(2-chlorophenyl)-4-carboxypiperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.
1146894-87-2
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Basic information
- Product Name: 1-Boc-4-(2-chlorophenyl)-4-carboxypiperidine
- Synonyms: 1-Boc-4-(2-chlorophenyl)-4-carboxypiperidine;1-(tert-Butoxycarbonyl)-4-(2-chlorophenyl)piperidine-4-carboxylic acid
- CAS NO:1146894-87-2
- Molecular Formula: C17H22ClNO4
- Molecular Weight: 339.81388
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1146894-87-2.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: 1-Boc-4-(2-chlorophenyl)-4-carboxypiperidine(CAS DataBase Reference)
- NIST Chemistry Reference: 1-Boc-4-(2-chlorophenyl)-4-carboxypiperidine(1146894-87-2)
- EPA Substance Registry System: 1-Boc-4-(2-chlorophenyl)-4-carboxypiperidine(1146894-87-2)
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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: 1146894-87-2(Hazardous Substances Data)
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1146894-87-2 Usage
Chemical structure
A derivative of piperidine with a tert-butoxycarbonyl group and a chlorophenyl groupTert-butoxycarbonyl group
A bulky ester group that can protect the carboxylic acid group during synthesisChlorophenyl group
A phenyl ring with a chlorine atom, which can influence the compound's propertiesCarboxylic acid group
Can form esters and amides, useful for further chemical reactionsPiperidine ring
A six-membered nitrogen-containing ring that can provide biological activity in drug candidatesOrganic synthesis
Used as a building block for the synthesis of other compoundsPharmaceutical research
Potentially used in the development of new drugs due to its versatile structure and functional groupsBiological activity
The presence of the piperidine ring may contribute to the compound's biological activity in some drug candidatesReactivity
Can undergo reactions such as esterification and amide formation due to the carboxylic acid groupStability
The tert-butoxycarbonyl group provides steric hindrance, which can protect the carboxylic acid group from unwanted reactionsSolubility
May be soluble in organic solvents such as ethanol, methanol, or acetoneMelting point
The exact melting point is not provided, but it is expected to be relatively high due to the presence of the bulky tert-butoxycarbonyl group and the aromatic chlorophenyl groupSynthesis
The compound can be synthesized through various chemical reactions, such as the reaction of a piperidine derivative with a chlorophenyl carboxylic acid derivative in the presence of a coupling agentPurity
The purity of the compound can be determined using techniques like high-performance liquid chromatography (HPLC) or mass spectrometry (MS)Safety
As with any chemical compound, proper handling and storage are necessary to avoid potential hazards. It is important to follow safety guidelines and use appropriate personal protective equipment (PPE) when working with 1-(Tert-butoxycarbonyl)-4-(2-chlorophenyl)piperidine-4-carboxylic acid.Check Digit Verification of cas no
The CAS Registry Mumber 1146894-87-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,8,9 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.Calculate Digit Verification of CAS Registry Number 1146894-87:
(9*1)+(8*1)+(7*4)+(6*6)+(5*8)+(4*9)+(3*4)+(2*8)+(1*7)=192
192 % 10 = 2
So 1146894-87-2 is a valid CAS Registry Number.
1146894-87-2Upstream product
1146894-87-2Downstream Products
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1-Boc-4-(2-chlorophenyl)-4-carboxypiperidine
