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355841-11-1

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355841-11-1 Usage

Uses

(Z)-Desbutyl Lumefantrine is a metabolite of Lumefantrine (L474000).

Check Digit Verification of cas no

The CAS Registry Mumber 355841-11-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,5,8,4 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 355841-11:
(8*3)+(7*5)+(6*5)+(5*8)+(4*4)+(3*1)+(2*1)+(1*1)=151
151 % 10 = 1
So 355841-11-1 is a valid CAS Registry Number.

355841-11-1SDS

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 2-(butylamino)-1-[(9E)-2,7-dichloro-9-[(4-chlorophenyl)methylidene]fluoren-4-yl]ethanol

1.2 Other means of identification

Product number -
Other names -

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:355841-11-1 SDS

355841-11-1Downstream Products

355841-11-1Relevant articles and documents

Synthetic method of benzofluorenol-D9

-

, (2020/07/13)

The invention provides a synthesis method of benzofluorenol-D9, which comprises the following steps: 1) in the presence of anhydrous aluminum chloride, carrying out Friedel-Crafts reaction on a compound 1 and chloroacetyl chloride to obtain a compound 2; 2) performing reduction reaction on the compound 2 and sodium borohydride to obtain a compound 3; 3) performing substitution reaction on the compound 3 and n-butylamine to obtain a compound 4; 4) in the presence of alkali, carrying out condensation reaction on the compound 4 and p-chlorobenzaldehyde to prepare a compound 5; and 5) in the presence of potassium carbonate, subjecting the compound 5 and deuterated n-bromobutane-D9 to a substitution reaction so as to prepare benzofluorenol-D9. According to the method, the commercially availabledeuterated n-bromobutane-D9 is used as the deuterated raw material for the first time, the deuterated benzofluorenol-D9 is finally synthesized through a series of reactions, use of di-n-butylamine-D9is avoided, the deuterated raw material with high price is used as the last step of reaction raw material in the route, and cost reduction is facilitated.

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