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143878-20-0

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  • 2-[(6,11-Dihydro-5H-dibenz[b,e]azepin-6-yl)-methyl]-1H-isoindole-1,3(2H)-dione

    Cas No: 143878-20-0

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143878-20-0 Usage

Chemical Properties

Off-White Solid

Uses

6-(Phthalimidomethyl)-6,11-dihydro-5h-dibenz[b,e]azepine (cas# 143878-20-0) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 143878-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,8,7 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 143878-20:
(8*1)+(7*4)+(6*3)+(5*8)+(4*7)+(3*8)+(2*2)+(1*0)=150
150 % 10 = 0
So 143878-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C23H18N2O2/c26-22-18-10-4-5-11-19(18)23(27)25(22)14-21-17-9-3-1-7-15(17)13-16-8-2-6-12-20(16)24-21/h1-12,21,24H,13-14H2

143878-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(Phthalimidomethyl)-6,11-dihydro-5h-dibenz[b,e]azepine

1.2 Other means of identification

Product number -
Other names 2-(6,11-dihydro-5H-benzo[c][1]benzazepin-6-ylmethyl)isoindole-1,3-dione

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:143878-20-0 SDS

143878-20-0Relevant articles and documents

The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine

Roszkowski, Piotr,Maurin,Czarnocki, Zbigniew

, p. 1509 - 1513 (2015)

A simple enantioselective synthetic procedure for the preparation of mianserin and epinastine in optically pure form is described. The key step in the synthetic pathway is the asymmetric reduction of the cyclic imine using asymmetric transfer hydrogenation conditions.

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