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6237-22-5

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6237-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6237-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,3 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6237-22:
(6*6)+(5*2)+(4*3)+(3*7)+(2*2)+(1*2)=85
85 % 10 = 5
So 6237-22-5 is a valid CAS Registry Number.

6237-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N',N'-dimethyl-N-(2-nitroacridin-9-yl)propane-1,3-diamine

1.2 Other means of identification

Product number -
Other names C 264

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:6237-22-5 SDS

6237-22-5Downstream Products

6237-22-5Relevant articles and documents

REACTIONS AT C-9 OF ACRIDINE DERIVATIVES. PART XXVIII. KINETICS OF 1-, 2-, 3- AND 4-NITRO-9-AMINOACRIDINE SYNTHESES. SUBSTITUENT EFFECT OF THE NO2 GROUP DURING AMINOLYSIS

Kunikowski, Antoni,Ledochowski, Andrzej

, p. 435 - 445 (2007/10/02)

Spectrophotometric studies on dimethylaminopropylamine (DMAPA) reactions with 1-, 2-, 3- and 4-nitro-9-chloro(phenoxy)acridines were carried out in DMSO and in xylene.Reactions in DMSO were of the second order, with nitro isomers reacting in the sequence of 2>4>1ca.3; reactions in xylene were of the third order, with nitro isomers reacting in the sequence of 2>1>4>3; α-pyridone and triethylamine produced no catalytic effect.These data might suggest strong "para" type nitro activation for the 2-nitro isomer and significant steric interactions by nitro group to 1-nitro isomer aminolysis.

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