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Benzenemethanamine, N-(2-methylbutyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60508-94-3

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60508-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60508-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,0 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60508-94:
(7*6)+(6*0)+(5*5)+(4*0)+(3*8)+(2*9)+(1*4)=113
113 % 10 = 3
So 60508-94-3 is a valid CAS Registry Number.

60508-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-2-methylbutan-1-amine

1.2 Other means of identification

Product number -
Other names Benzenemethanamine,N-(2-methylbutyl)

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:60508-94-3 SDS

60508-94-3Downstream Products

60508-94-3Relevant academic research and scientific papers

Polyoxometalate-Driven Ease Conversion of Valuable Furfural to trans- N, N-4,5-Diaminocyclopenten-2-ones

Fountoulaki, Stella,Lykakis, Ioannis N.,Tzani, Marina A.

, (2022/02/10)

We investigated the catalytic efficacy of silicotungstic acid (H4SiW12O40) polyoxometalate (POM) toward the reaction between furfural and amines that selectively yields trans-N,N-4,5-substituted-diaminocyclopenten-2-ones (trans-DACPs). H4SiW12O40 facilita

A CONVENIENT SYNTHESIS OF UNSYMMETRICAL SECONDARY AMINES. IN SITU FORMATION OF UNSTABLE FORMALDEHYDE IMINES.

Overman, Larry E.,Burk, Robert M.

, p. 1635 - 1638 (2007/10/02)

The monoalkylation of aliphatic and aromatic primary amines can be accomplished by the reaction of organolithium or grignard reagents with N-(cyanomethyl) or N-(aminomethyl) derivatives.

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