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3-(4-FLUOROPHENOXY)PROPAN-1-AMINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

148941-98-4

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148941-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148941-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,9,4 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 148941-98:
(8*1)+(7*4)+(6*8)+(5*9)+(4*4)+(3*1)+(2*9)+(1*8)=174
174 % 10 = 4
So 148941-98-4 is a valid CAS Registry Number.

148941-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-fluorophenoxy)propan-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:148941-98-4 SDS

148941-98-4Upstream product

148941-98-4Downstream Products

148941-98-4Relevant academic research and scientific papers

Nucleophilic Substitution at the Guanidine Carbon Center via Guanidine Cyclic Diimide Activation

An, Taeyang,Lee, Yan

supporting information, p. 9163 - 9167 (2021/11/24)

Despite the electron-deficient nature of the guanidine carbon centers, nucleophilic reactions at these sites have been underdeveloped because of the resonance stabilization of the guanidine group. We propose a guanidine C-N bond substitution strategy entailing the formation of guanidine cyclic diimide (GCDI) structures, which effectively destabilize the resonance structure of the guanidine group. In the presence of acid additives, the guanidine carbon center of GCDIs undergoes nucleophilic substitution reactions with various amines and alcohols.

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