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22302-58-5

22302-58-5

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22302-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22302-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,0 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22302-58:
(7*2)+(6*2)+(5*3)+(4*0)+(3*2)+(2*5)+(1*8)=65
65 % 10 = 5
So 22302-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H12ClNO/c1-9(14)13(16)15-12-8-4-6-10-5-2-3-7-11(10)12/h2-9H,1H3,(H,15,16)/t9-/m1/s1

22302-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-naphthalen-1-ylpropanamide

1.2 Other means of identification

Product number -
Other names Propanamide,N-(1-naphthyl)-2-chloro

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:22302-58-5 SDS

22302-58-5Downstream Products

22302-58-5Relevant articles and documents

Synthesis of novel N-(naphthalen-1-yl)propanamide derivatives and evaluation their antimicrobial activity

Evren, Asaf E.,Yurttas, Leyla,Y?lmaz-Cankilic, Meral

, p. 158 - 164 (2020)

New N-(naphthalen-1-yl)propanamide was synthesized and studied for their antimicrobial activity. The final compounds were procured by reacting N-(naphthalen-1-yl)propanamide with some 2-mercapto aryl or dithiocarbamate salt derivatives. Their structures w

Triamine derivatives and their acid-addition salts

-

, (2008/06/13)

A triamine derivative of the formula (I) ψψ ψwherein Ar1 and Ary are carbocyclic or heterocyclic single ring or fused ring aromatic groups, R1, Ry and R3 are hydrogen, lower alkyl, aryl aryl-alkyl, aryl-alkyloxycarbonyl, alkyloxycarbonyl or acyl, and A1 and Ay are lower alkylene groups optionally substituted by oxo, exhibits a high N-methyl-D-aspartic acid (NMDA) receptor antagonistic effect and are therefore useful as a medicine for nerve degeneration diseases.ψ

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