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6622-25-9

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6622-25-9 Usage

Belongs to the group of ethanolamines

Contains both an amine and an alcohol functional group

Derivative of ethanol

Has a pentylamine group attached to the ethylamine group

Usage

Building block in the synthesis of other organic compounds, solvent or additive in industrial processes

Versatility

Can be used in pharmaceuticals, cosmetics, and other chemical applications

Check Digit Verification of cas no

The CAS Registry Mumber 6622-25-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6622-25:
(6*6)+(5*6)+(4*2)+(3*2)+(2*2)+(1*5)=89
89 % 10 = 9
So 6622-25-9 is a valid CAS Registry Number.

6622-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(pentan-3-ylamino)ethanol

1.2 Other means of identification

Product number -
Other names N-(2-hydroxyethyl)-N-(3-pentyl)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:6622-25-9 SDS

6622-25-9Downstream Products

6622-25-9Relevant articles and documents

Selective Palladium(II)-Catalyzed Carbonylation of Methylene β-C?H Bonds in Aliphatic Amines

Cabrera-Pardo, Jaime R.,Trowbridge, Aaron,Nappi, Manuel,Ozaki, Kyohei,Gaunt, Matthew J.

supporting information, p. 11958 - 11962 (2017/09/20)

Palladium(II)-catalyzed C?H carbonylation reactions of methylene C?H bonds in secondary aliphatic amines lead to the formation of trans-disubstituted β-lactams in excellent yields and selectivities. The generality of the C?H carbonylation process is aided by the action of xantphos-based ligands and is important in securing good yields for the β-lactam products.

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