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146935-39-9

epocarbazolin A is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 4-(hydroxymethyl)-7-methyl-8-[3-methyl-3-(3-methylbutyl)oxiran-2-yl]-9H-carbazole-1,6-diol

    Cas No: 146935-39-9

  • USD $ 1.9-2.9 / Gram

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  • 146935-39-9 Structure

  • Basic information

    1. Product Name: epocarbazolin A
    2. Synonyms: epocarbazolin A
    3. CAS NO:146935-39-9
    4. Molecular Formula: C22H27NO4
    5. Molecular Weight: 369.458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146935-39-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 636.4°Cat760mmHg
    3. Flash Point: 338.7°C
    4. Appearance: /
    5. Density: 1.283g/cm3
    6. Vapor Pressure: 4.52E-17mmHg at 25°C
    7. Refractive Index: 1.675
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: epocarbazolin A(CAS DataBase Reference)
    11. NIST Chemistry Reference: epocarbazolin A(146935-39-9)
    12. EPA Substance Registry System: epocarbazolin A(146935-39-9)

  • 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: 146935-39-9(Hazardous Substances Data)

146935-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146935-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,3 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 146935-39:
(8*1)+(7*4)+(6*6)+(5*9)+(4*3)+(3*5)+(2*3)+(1*9)=159
159 % 10 = 9
So 146935-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H27NO4/c1-11(2)7-8-22(4)21(27-22)17-12(3)16(26)9-14-18-13(10-24)5-6-15(25)20(18)23-19(14)17/h5-6,9,11,21,23-26H,7-8,10H2,1-4H3

146935-39-9SDS

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-(hydroxymethyl)-7-methyl-8-[3-methyl-3-(3-methylbutyl)oxiran-2-yl]-9H-carbazole-1,6-diol

1.2 Other means of identification

Product number -
Other names Epocarbazolin A

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:146935-39-9 SDS

146935-39-9Downstream Products

146935-39-9Relevant articles and documents

Transition metals in organic synthesis - Part 83#: Synthesis and pharmacological potential of carbazoles

Choi, Taylor A.,Czerwonka, Regina,Forke, Ronny,Jaeger, Anne,Knoell, Jan,Krahl, Micha P.,Krause, Tilo,Reddy, Kethiri R.,Franzblau, Scott G.,Knoelker, Hans-Joachim

, p. 374 - 385 (2008/12/23)

A series of carbazole derivatives with promising pharmacological properties has been prepared using either an iron-mediated or a palladium-catalyzed synthetic approach. The carbazole alkaloids carbazoquinocin C, carbazomadurin A and B, epocarbazolin A and

First total synthesis of (±)-epocarbazolin A and epocarbazolin B, and asymmetric synthesis of (-)-epocarbazolin A via Shi epoxidation

Kn?ll, Jan,Kn?lker, Hans-Joachim

, p. 6079 - 6082 (2007/10/03)

Epoxidation of the trisilyl-protected carbazomadurins A and B with dimethyldioxirane followed by desilylation provides a simple route to racemic epocarbazolin A and a non-diastereoselective access to epocarbazolin B. The Shi epoxidation has been applied t

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