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6291-85-6

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6291-85-6 Usage

Chemical Properties

CLEAR COLOURLESS LIQUID

Uses

It is employed as an intermediate used in the production of dyestuff and cosmetics. It is also used to partially open the rigid oxetane chain and to identify Hsp70 modulators.

Application

3-Ethoxypropylamine is mainly used for the synthesis of disperse red 90.

Check Digit Verification of cas no

The CAS Registry Mumber 6291-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6291-85:
(6*6)+(5*2)+(4*9)+(3*1)+(2*8)+(1*5)=106
106 % 10 = 6
So 6291-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H13NO/c1-2-7-5-3-4-6/h2-6H2,1H3/p+1

6291-85-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Packaging
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  • Detail
  • Alfa Aesar

  • (B23694)  3-Ethoxypropylamine, 99%   

  • 6291-85-6

  • 100g

  • 421.0CNY

  • Detail
  • Alfa Aesar

  • (B23694)  3-Ethoxypropylamine, 99%   

  • 6291-85-6

  • 500g

  • 1854.0CNY

  • Detail
  • Aldrich

  • (239437)  3-Ethoxypropylamine  99%

  • 6291-85-6

  • 239437-100G

  • 321.75CNY

  • Detail

6291-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Ethoxypropylamine

1.2 Other means of identification

Product number -
Other names 3-ethoxypropan-1-amine

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:6291-85-6 SDS

6291-85-6Relevant articles and documents

Preparation method of 3-ethoxypropylamine

-

Paragraph 0016; 0020-0025, (2019/03/08)

The invention discloses a preparation method of 3-ethoxypropylamine. The preparation method comprises the following steps: 1) adding a catalyst A and ethanol into a reactor; 2) controlling the temperature of the reactor and dripping acrylonitrile; 3) preparing 3-ethoxy propionitrile with the content of more than 97%; 4) hydrogenating the prepared 3-ethoxy propionitrile in the presence of a catalyst B, hydrogen and an inhibitor; and 5) after the hydrogenation is qualified, carrying out vacuum vacuum distillation to obtain a finished product with a content greater than 99.5%. The preparation method has high selectivity, and excessive ethanol and the catalysts A and B in the process can be recycled, thus further reducing the production cost and reducing the discharge amount of waste liquid.

2-aminopyridine derivatives and combinatorial libraries thereof

-

, (2008/06/13)

The present invention relates to novel 2-aminopyridine derivative compounds of the following formula: wherein R1to R5have the meanings provided herein. The invention further relates to combinatorial libraries containing two or more such compounds, as well as methods of preparing 2-aminopyridine derivative compounds.

Aldose epimerization by Ni(II): effect of ether-containig alkylenediamine ligands

Osanai, Shuichi,Inaba, Kiyoshi,Yoshikawa, Sadao

, p. 289 - 295 (2007/10/02)

Several N-substituted ethylenediamine (en) Ni(II) derivatives containing ether linkages were prepared in order to study the effect of ligand structure on C-2 epimerization of aldohexoses.The reagent consisted of a Ni(II)-alkyenediamine derivative in methanol.The presence of ether linkages in the ligand increased the solubilty of the complexes, and resulted in an increase in the rate of epimerization.Epimerization occured rapidly under mild conditions, and the same equilibrium point was reached regardless of whether the reaction was started from glucose or mannose.Among the ligands studied, N,N'-dialkylethylenediamine was the most effective in C-2 epimerization.

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