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Phenol, 2-[(dipropylamino)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60460-59-5

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60460-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60460-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,6 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60460-59:
(7*6)+(6*0)+(5*4)+(4*6)+(3*0)+(2*5)+(1*9)=105
105 % 10 = 5
So 60460-59-5 is a valid CAS Registry Number.

60460-59-5SDS

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 2-[(dipropylamino)methyl]phenol

1.2 Other means of identification

Product number -
Other names Phenol,2-[(dipropylamino)methyl]

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:60460-59-5 SDS

60460-59-5Downstream Products

60460-59-5Relevant academic research and scientific papers

The modified-Mannich reaction: Conversion of arylboronic acids and subsequent coupling with paraformaldehyde and amines toward the one-pot synthesis of Mannich bases and benzoxazines

Liu, Juan,Yuan, Gaoqing

supporting information, p. 1470 - 1473 (2017/03/23)

A modified Mannich reaction has been developed for the synthesis of Mannich bases and benzoxazines via the oxidative hydroxylation of arylboronic acids and subsequent coupling with paraformaldehyde and amines in one pot. This modified Mannich reaction is easily carried out to afford the target products in good to excellent yields and tolerates a variety of functional groups.

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