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6305-56-2

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6305-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6305-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6305-56:
(6*6)+(5*3)+(4*0)+(3*5)+(2*5)+(1*6)=82
82 % 10 = 2
So 6305-56-2 is a valid CAS Registry Number.

6305-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-cyanoethyl(2-hydroxyethyl)amino]propanenitrile

1.2 Other means of identification

Product number -
Other names 3-(2-cyanoethyl-(2-hydroxyethyl)amino)propanenitrile

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:6305-56-2 SDS

6305-56-2Relevant articles and documents

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Kreevoy,M.M.,Oh,S.-W.

, p. 4805 - 4810 (1973)

-

Convergent synthesis of polynitrile and/or polyamine dendrimers through hydroaminomethylation and Michael addition

Beigi, Maryam,Ricken, Stefan,Mueller, Kai Sven,Koc, Fikret,Eilbracht, Peter

supporting information; experimental part, p. 1482 - 1492 (2011/04/22)

A general concept for a versatile convergent synthesis ofpolynitrile and/or polyamine dendrimers has been developed by applying Voegtle's procedure in combination with thetandem hydroformylation/reductive amination sequence, known as hydroaminomethylation

Aqueous aza-michael reaction of conjugated alkenes: Toward spermine

Joshi, Jigar H.,Saiyed, Akeel S.,Bedekar, Ashutosh V.

experimental part, p. 2857 - 2863 (2010/11/18)

An aqueous aza-Michael reaction is efficiently achieved with excellent conversions without any additives. The method works very well on a molar scale with selectively for aliphatic amines. An intermediate for spermine is also made by this green process.

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