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885274-98-6

N-CBZ-4-CHLORO-PIPERIDINE, also known as 4-chloromethylbenzhydryl piperidine, is a chemical compound that belongs to the family of piperidine derivatives. It is commonly used in organic synthesis as a building block for various pharmaceutical and agrochemical products. N-CBZ-4-CHLORO-PIPERIDINE is an important intermediate in the synthesis of certain drugs and is also used as a reagent in chemical reactions.
Used in Pharmaceutical Industry:
N-CBZ-4-CHLORO-PIPERIDINE is used as a key intermediate for the synthesis of antipsychotic and antidepressant medications. Its role in the development of these medications is crucial, as it contributes to the creation of effective treatments for mental health disorders.
Used in Organic Synthesis:
N-CBZ-4-CHLORO-PIPERIDINE is used as a building block in the synthesis of various pharmaceutical and agrochemical products. Its versatility in organic synthesis allows for the development of a wide range of compounds with different applications.
Used as a Reagent in Chemical Reactions:
N-CBZ-4-CHLORO-PIPERIDINE is utilized as a reagent in various chemical reactions, facilitating the formation of desired products and aiding in the advancement of chemical research and development.
It is important to handle N-CBZ-4-CHLORO-PIPERIDINE with care, as it can be hazardous if not used properly. Proper safety measures should be taken to ensure the safe handling and use of this chemical compound.

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  • 885274-98-6 Structure

  • Basic information

    1. Product Name: N-CBZ-4-CHLORO-PIPERIDINE
    2. Synonyms: N-CBZ-4-CHLORO-PIPERIDINE;Benzyl 4-chloropiperidine-1-carboxylate
    3. CAS NO:885274-98-6
    4. Molecular Formula: C13H16ClNO2
    5. Molecular Weight: 253.72
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 885274-98-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 379.7±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.21±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -2.82±0.40(Predicted)
    10. CAS DataBase Reference: N-CBZ-4-CHLORO-PIPERIDINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-CBZ-4-CHLORO-PIPERIDINE(885274-98-6)
    12. EPA Substance Registry System: N-CBZ-4-CHLORO-PIPERIDINE(885274-98-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36
    3. Safety Statements: 26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 885274-98-6(Hazardous Substances Data)

885274-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 885274-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 885274-98:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*4)+(2*9)+(1*8)=226
226 % 10 = 6
So 885274-98-6 is a valid CAS Registry Number.

885274-98-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 4-chloropiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-N-CBZ-4-CHLOROPIPERIDINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:885274-98-6 SDS

885274-98-6Relevant articles and documents

Process method for synthesizing N-substituted piperidine-4-boric acid

-

Paragraph 0026, (2020/06/17)

The invention relates to an organic compound synthesis method, and relates to a process method for synthesizing N-substituted piperidine-4-boric acid, which comprises the following steps of: reactingN-substituted piperidine-4-alcohol used as a raw material with thionyl chloride and organic alkali in a solvent to generate N-substituted piperidine-4-chlorine, reacting the N-substituted piperidine-4-chlorine used as a raw material with lithium metal and bis (N, N-dimethylamino) borane halide in a solvent, quenching and acidifying to obtain N-substituted piperidine-4-boric acid. The process method has the advantages of originality, low cost, safety and mild reaction conditions, avoids the dangerous reaction that other patented methods adopt expensive palladium hydroxide hydrogenation, has potential cost advantage and safety advantage, and is suitable for industrial scale-up production.

A method for the selective hydrogenation of alkenyl halides to alkyl halides

King, Sandra M.,Ma, Xiaoshen,Herzon, Seth B.

supporting information, p. 6884 - 6887 (2014/06/09)

A general method for the selective hydrogenation of alkenyl halides to alkyl halides is described. Fluoro, chloro, bromo, iodo, and gem-dihaloalkenes are viable substrates for the transformation. The selectivity of the hydrogenation is consistent with reduction by a hydrogen atom transfer pathway.

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