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3,7-bis(morpholin-4-ylmethyl)-10H-phenothiazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85689-73-2

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85689-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85689-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,8 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85689-73:
(7*8)+(6*5)+(5*6)+(4*8)+(3*9)+(2*7)+(1*3)=192
192 % 10 = 2
So 85689-73-2 is a valid CAS Registry Number.

85689-73-2SDS

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 4-[[7-(morpholin-4-ylmethyl)-10H-phenothiazin-3-yl]methyl]morpholine

1.2 Other means of identification

Product number -
Other names di(morpholinomethyl)-3,7 phenothiazine

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:85689-73-2 SDS

85689-73-2Downstream Products

85689-73-2Relevant academic research and scientific papers

Aminomethylation of phenothiazine and phenoxazine . Chemical and pharmacological studies

Vierfond,Lehuede,Miocque

, p. 35 - 40 (2007/10/02)

Phenothiazine and phenoxazine are converted to aminomethyl derivatives in position 3 or 3 and 7. Experimental conditions for mono or disubstitutions, and structure of products are studied. A 1-substituted derivative of phenothiazine is described. Pharmacological screening of main derivatives of phenothiazine shows low activity on CNS, small inhibition of staphylococcus and colibacillus but no parasiticidal action.

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