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20900-22-5

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20900-22-5 Usage

Structure

Brominated derivative of naphthalene with a bromine atom and an ethoxy group attached to the 4-position of the naphthalene ring

Usage

Reagent in organic synthesis, building block for the synthesis of various pharmaceutical and agrochemical compounds

Properties

Aromatic

Handling precautions

Potentially hazardous if not properly handled and stored.

Check Digit Verification of cas no

The CAS Registry Mumber 20900-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,0 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20900-22:
(7*2)+(6*0)+(5*9)+(4*0)+(3*0)+(2*2)+(1*2)=65
65 % 10 = 5
So 20900-22-5 is a valid CAS Registry Number.

20900-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-ethoxynaphthalene

1.2 Other means of identification

Product number -
Other names 4-bromo-1-ethoxynaphthalene

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:20900-22-5 SDS

20900-22-5Downstream Products

20900-22-5Relevant articles and documents

Facile synthesis of lipophilic δ-amino acid conjugates from 4-alkoxy-dithionaphthoic acids

Worth, Anna C.,Needham, Catherine E.,Franklin, Donald B.,Lampkins, Andrew J.

experimental part, p. 2694 - 2706 (2012/07/28)

(Chemical Equation Presented) Novel 4-alkoxy-dithionaphthoic acids were prepared and shown to be valuable synthons for δ-amino acid conjugates. These dithioacids are efficiently synthesized and purified, stable to storage, and easily derivatized to facilitate thioacylation chemistry. To this end, we have demonstrated dithionaphthoic acids (6) to successfully undergo coupling with both protected and unprotected amino acids, giving rise to stable thioamide conjugates (8 and 9). Copyright Taylor & Francis Group, LLC.

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