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Piperidine-4-boronic acid is a crystalline solid chemical compound belonging to the class of boronic acids, with the chemical formula C5H10BNO2. It is commonly used as a reagent in organic synthesis, particularly for the formation of carbon-carbon and carbon-nitrogen bonds. The boron atom in this compound provides unique reactivity and selectivity in various chemical reactions, making it a valuable tool in synthetic chemistry. Its mild and efficient reaction conditions make it a popular choice for a wide range of applications in the field of organic chemistry.

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  • 120347-72-0 Structure
  • Basic information

    1. Product Name: PIPERIDINE-4-BORONIC ACID
    2. Synonyms: PIPERIDINE-4-BORONIC ACID;Boronic acid, 4-piperidinyl-
    3. CAS NO:120347-72-0
    4. Molecular Formula: C5H12BNO2
    5. Molecular Weight: 128.97
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120347-72-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 280.8±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.08±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.96±0.20(Predicted)
    10. CAS DataBase Reference: PIPERIDINE-4-BORONIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: PIPERIDINE-4-BORONIC ACID(120347-72-0)
    12. EPA Substance Registry System: PIPERIDINE-4-BORONIC ACID(120347-72-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 120347-72-0(Hazardous Substances Data)

120347-72-0 Usage

Uses

Used in Organic Synthesis:
Piperidine-4-boronic acid is used as a reagent for the formation of carbon-carbon and carbon-nitrogen bonds, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
Piperidine-4-boronic acid is used as a key intermediate in the production of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemicals:
PIPERIDINE-4-BORONIC ACID is utilized in the synthesis of agrochemicals, playing a role in the development of pesticides and other agricultural chemicals to improve crop protection and yield.
Used in Materials Science:
Piperidine-4-boronic acid is employed in the field of materials science for the synthesis of new materials with specific properties, such as conductivity, strength, or flexibility, for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 120347-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,4 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120347-72:
(8*1)+(7*2)+(6*0)+(5*3)+(4*4)+(3*7)+(2*7)+(1*2)=90
90 % 10 = 0
So 120347-72-0 is a valid CAS Registry Number.

120347-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name piperidin-4-ylboronic acid

1.2 Other means of identification

Product number -
Other names Boronic acid,4-piperidinyl

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:120347-72-0 SDS

120347-72-0Downstream Products

120347-72-0Relevant articles and documents

Hydrogenation of Borylated Arenes

Wollenburg, Marco,Moock, Daniel,Glorius, Frank

supporting information, p. 6549 - 6553 (2019/01/04)

A cis-selective hydrogenation of abundant aryl boronic acids and their derivatives catalyzed by rhodium cyclic (alkyl)(amino)carbene (Rh–CAAC) is reported. The reaction tolerates a variety of boron-protecting groups and provides direct access to a broad s

NEW PREPARATION OF AMINOBORONIC ACIDS

Dicko, Amadou,Montury, Michel,Baboulene, Michel

, p. 459 - 464 (2007/10/02)

A new preparation of aminoboronic acids, starting from N-trimethylsylil derivatives of olefinic amines and utilizing the hydroboration reaction, is described as a ''one pot'' reaction.

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