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40226-15-1

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40226-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40226-15-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,2 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40226-15:
(7*4)+(6*0)+(5*2)+(4*2)+(3*6)+(2*1)+(1*5)=71
71 % 10 = 1
So 40226-15-1 is a valid CAS Registry Number.

40226-15-1SDS

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 3-(3-aminopropylamino)propan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:40226-15-1 SDS

40226-15-1Relevant articles and documents

Template-directed syntheses of rigid oligorotaxanes under thermodynamic control

Belowich, Matthew E.,Valente, Cory,Stoddart, J. Fraser

supporting information; experimental part, p. 7208 - 7212 (2010/12/18)

Strategically placing secondary dialkyl-ammonium recognition sites at the magic distance of 3.5 A apart in the dumbbell components of a series of oligorotaxanes (see picture) renders otherwise conformationally floppy [n]rotaxanes rigid and rodlike. These oligorotaxanes form with near-quantitative conversion under thermodynamic control using dynamic covalent chemistry.

Expedient protocol for solid-phase synthesis of secondary and tertiary amines

Olsen, Christian A.,Witt, Matthias,Jaroszewski, Jerzy W.,Franzyk, Henrik

, p. 1935 - 1938 (2007/10/03)

Equation presented. An expedient solid-phase synthetic approach to secondary and tertiary amines was developed. The protocol employs conversion of resin-bound amino alcohols to the corresponding iodides, followed by iodide displacement with primary or sec

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