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1-Propanamine, N-ethyl-2-methyl-N-(2-methylpropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18677-85-5

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18677-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18677-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,7 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18677-85:
(7*1)+(6*8)+(5*6)+(4*7)+(3*7)+(2*8)+(1*5)=155
155 % 10 = 5
So 18677-85-5 is a valid CAS Registry Number.

18677-85-5SDS

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 N-ethyl-2-methyl-N-(2-methylpropyl)propan-1-amine

1.2 Other means of identification

Product number -
Other names diisobutylethylamine

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:18677-85-5 SDS

18677-85-5Downstream Products

18677-85-5Relevant academic research and scientific papers

An efficient synthesis of tertiary amines from nitriles in aprotic solvents

Shares, Jonathan,Yehl, Jenna,Kowalsick, Amanda,Byers, Philip,Haaf, Michael P.

, p. 4426 - 4428 (2012)

Tertiary amines are utilized extensively as non-nucleophilic proton scavengers for a number of organic transformations. Herein we report the efficient syntheses of tertiary alkyl amines from their corresponding alkyl nitriles in the presence of a heterogeneous palladium catalyst and a source of dihydrogen in aprotic solvents. The reaction is atom economic, the conditions are mild, and the isolated yields are virtually quantitative. The degree of amine alkylation shows some solvent dependency; in polar protic solvents such as ethanol or methanol, the reaction affords a mixture of products with the secondary alkyl amine as the major product.

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