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24715-90-0

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24715-90-0 Usage

Uses

4-(1-Pyrrolidinyl)-1-butanamine is a useful reagent used in the preparation of imidazolidinedione derivatives used as antimalarial agents. A building block for organic synthesis.

Synthesis Reference(s)

Journal of the American Chemical Society, 95, p. 3038, 1973 DOI: 10.1021/ja00790a064

Check Digit Verification of cas no

The CAS Registry Mumber 24715-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,1 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24715-90:
(7*2)+(6*4)+(5*7)+(4*1)+(3*5)+(2*9)+(1*0)=110
110 % 10 = 0
So 24715-90-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H18N2/c9-5-1-2-6-10-7-3-4-8-10/h1-9H2

24715-90-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H50323)  4-(1-Pyrrolidinyl)-1-butylamine, 98%   

  • 24715-90-0

  • 1g

  • 673.0CNY

  • Detail
  • Alfa Aesar

  • (H50323)  4-(1-Pyrrolidinyl)-1-butylamine, 98%   

  • 24715-90-0

  • 5g

  • 3023.0CNY

  • Detail

24715-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1-Pyrrolidinyl)-1-butanamine

1.2 Other means of identification

Product number -
Other names 1-(4-AMINOBUTYL)PYRROLIDONE

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:24715-90-0 SDS

24715-90-0Downstream Products

24715-90-0Relevant articles and documents

Steric effects in the catalytic amination of γ-, δ-, and ε-glycols

Timofeev,Bazanov,Zubritskaya

, p. 1756 - 1761 (2017/02/19)

The amination of butane-1,4-diol, isomeric dipropylene glycols, and cyclohexane-1,4-diyldimethanol in the presence of nickel/copper/chromium catalysts has been studied. The effect of the initial glycol structure on the reaction selectivity has been estima

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