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N-tert-butylpyridine-3-sulfonaMide is a versatile chemical compound that is a sulfonamide derivative of pyridine, featuring a tert-butyl group attached to the nitrogen atom. It is recognized for its strong basicity and nucleophilic catalytic properties, which are instrumental in a range of organic reactions. Additionally, it serves as a building block in the pharmaceutical industry for the synthesis of diverse drug compounds, owing to its unique structure and reactivity.

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  • 17432-06-3 Structure
  • Basic information

    1. Product Name: N-tert-butylpyridine-3-sulfonaMide
    2. Synonyms: N-tert-butylpyridine-3-sulfonaMide
    3. CAS NO:17432-06-3
    4. Molecular Formula: C9H14N2O2S
    5. Molecular Weight: 214.28466
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17432-06-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: N-tert-butylpyridine-3-sulfonaMide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-tert-butylpyridine-3-sulfonaMide(17432-06-3)
    11. EPA Substance Registry System: N-tert-butylpyridine-3-sulfonaMide(17432-06-3)
  • 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: 17432-06-3(Hazardous Substances Data)

17432-06-3 Usage

Uses

Used in Organic Synthesis:
N-tert-butylpyridine-3-sulfonaMide is used as a catalyst for its strong basic and nucleophilic properties, facilitating various organic reactions and enhancing their efficiency and selectivity.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, N-tert-butylpyridine-3-sulfonaMide is utilized as a key building block in the synthesis of a variety of drug compounds, contributing to the development of new medications due to its unique structural and reactive attributes.

Check Digit Verification of cas no

The CAS Registry Mumber 17432-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,3 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17432-06:
(7*1)+(6*7)+(5*4)+(4*3)+(3*2)+(2*0)+(1*6)=93
93 % 10 = 3
So 17432-06-3 is a valid CAS Registry Number.

17432-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-butylpyridine-3-sulfonamide

1.2 Other means of identification

Product number -
Other names N-t-butylpyridine-3-sulphonamide

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:17432-06-3 SDS

17432-06-3Relevant articles and documents

Directed Metalation of Pyridinesulphonamides. Synthesis of Pyridine-fused Isothiazoles and 1,2-Oxathioles

Alo, Babajide I.,Familoni, Oluwole B.,Marsais, Francis,Queguiner, Guy

, p. 61 - 64 (2007/10/02)

4-Lithio-N-t-butylpyridine-3-sulphonamide reacted with benzophenone and carbon dioxide respectively to give the corresponding intermediates which on appropriate treatment gave isothiazolo-3-one 1,1-dioxides.Metalation of 2- and 4-(N,N-dialkylaminosulphonyl)pyridines with lithium diisopropylamide (LDA) gave anions which reacted with benzophenone to give carbinols which thermally cyclised to 1,2-oxathiolopyridine and 1,2-oxathiolopyridine respectively.

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