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143878-20-0

6-(Phthalimidomethyl)-6,11-dihydro-5H-dibenz[b,e]azepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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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

  • USD $ 1.2-5.0 / Kiloliter

  • 5 Kiloliter

  • 3000 Metric Ton/Month

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  • 6-(Phthalimidomethyl)-6,11-dihydro-5H-dibenz[b,e]azepine

    Cas No: 143878-20-0

  • No Data

  • 25 Kilogram

  • 1 million Metric Ton/Year

  • COLORCOM LTD.
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  • 143878-20-0 Structure

  • Basic information

    1. Product Name: 6-(Phthalimidomethyl)-6,11-dihydro-5H-dibenz[b,e]azepine
    2. Synonyms: 6-(PHTHALIMIDOMETHYL)-6,11-DIHYDRO-5H-DIBENZ-B,EAZEPINE;2-[(6,11-Dihydro-5H-dibenz[b,e]azepin-6-yl)Methyl]-1H-isoindole-1,3(2H)-dione;6-(PhthaliMidoMethyl)-5,6-dihydroMorphanthridine;2-((6,11-Dihydro-5H-dibenzo[b,e]azepin-6-yl)Methyl)isoindoline-1,3-dione;6-(Phthalimidomethyl)-6,11-dihydro-5H-dibenz-[b,e]azepine (PMDAP)
    3. CAS NO:143878-20-0
    4. Molecular Formula: C23H18N2O2
    5. Molecular Weight: 354.4
    6. EINECS: 1806241-263-5
    7. Product Categories: Amines;Aromatics;Heterocycles;Intermediates
    8. Mol File: 143878-20-0.mol
    9. Article Data: 1

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 557.301 °C at 760 mmHg
    3. Flash Point: 290.845 °C
    4. Appearance: Off-white solid
    5. Density: 1.284 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.662
    8. Storage Temp.: -20°C Freezer, Under inert atmosphere
    9. Solubility: Acetonitrile (Very Slightly), DMSO (Slightly)
    10. PKA: 3.94±0.40(Predicted)
    11. CAS DataBase Reference: 6-(Phthalimidomethyl)-6,11-dihydro-5H-dibenz[b,e]azepine(CAS DataBase Reference)
    12. NIST Chemistry Reference: 6-(Phthalimidomethyl)-6,11-dihydro-5H-dibenz[b,e]azepine(143878-20-0)
    13. EPA Substance Registry System: 6-(Phthalimidomethyl)-6,11-dihydro-5H-dibenz[b,e]azepine(143878-20-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 143878-20-0(Hazardous Substances Data)

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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