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5118-29-6

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5118-29-6 Usage

Uses

Antidepressant.

Therapeutic Function

Antidepressant

Check Digit Verification of cas no

The CAS Registry Mumber 5118-29-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5118-29:
(6*5)+(5*1)+(4*1)+(3*8)+(2*2)+(1*9)=76
76 % 10 = 6
So 5118-29-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H25N/c1-21(2)19-13-7-5-10-17(19)16(12-9-15-22(3)4)18-11-6-8-14-20(18)21/h5-8,10-14H,9,15H2,1-4H3

5118-29-6SDS

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 3-(10,10-dimethylanthracen-9-ylidene)-N,N-dimethylpropan-1-amine

1.2 Other means of identification

Product number -
Other names Melitracen

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:5118-29-6 SDS

5118-29-6Downstream Products

5118-29-6Relevant articles and documents

Redesign of a Grignard-Based Active Pharmaceutical Ingredient (API) Batch Synthesis to a Flow Process for the Preparation of Melitracen HCl

Pedersen, Michael J.,Skovby, Tommy,Mealy, Michael J.,Dam-Johansen, Kim,Kiil, S?ren

, p. 228 - 235 (2018/02/23)

A Grignard-based batch process, for the preparation of Melitracen HCl, has been redesigned to fit a continuous reactor system. The Grignard addition is carried out at room temperature, with subsequent hydrolysis of the magnesium alkoxide intermediate followed by dehydration of the resulting alcohol. The product undergoes further workup by simple gravimetric phase separation and then crystallization with 2 M HCl in diethyl ether to afford pure Melitracen HCl. All steps in the laboratory setup were concatenated, and the setup was proven capable of producing a significant portion of the commercial quantities of Melitracen HCl. The flow setup profits from a reduced footprint, lower energy consumption, fewer synthetic steps, and reduced raw material usage compared to the batch process.

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