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133401-10-2

9H-pyrido[4,3,2-mn][1,3]thiazolo[4,5-b]acridin-9-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133401-10-2 Structure

  • Basic information

    1. Product Name: 9H-pyrido[4,3,2-mn][1,3]thiazolo[4,5-b]acridin-9-one
    2. Synonyms: 9H-Pyrido[4,3,2-mn][1,3]thiazolo[4,5-b]acridin-9-one; 9H-pyrido[4,3,2-mn]thiazolo[4,5-b]acridin-9-one
    3. CAS NO:133401-10-2
    4. Molecular Formula: C16H7N3OS
    5. Molecular Weight: 289.3113
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133401-10-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 619.1°C at 760 mmHg
    3. Flash Point: 328.2°C
    4. Appearance: N/A
    5. Density: 1.587g/cm3
    6. Vapor Pressure: 2.98E-15mmHg at 25°C
    7. Refractive Index: 1.862
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 9H-pyrido[4,3,2-mn][1,3]thiazolo[4,5-b]acridin-9-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 9H-pyrido[4,3,2-mn][1,3]thiazolo[4,5-b]acridin-9-one(133401-10-2)
    12. EPA Substance Registry System: 9H-pyrido[4,3,2-mn][1,3]thiazolo[4,5-b]acridin-9-one(133401-10-2)

  • 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: 133401-10-2(Hazardous Substances Data)

133401-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133401-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,4,0 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133401-10:
(8*1)+(7*3)+(6*3)+(5*4)+(4*0)+(3*1)+(2*1)+(1*0)=72
72 % 10 = 2
So 133401-10-2 is a valid CAS Registry Number.

133401-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name kuanoniamine A

1.2 Other means of identification

Product number -
Other names 6-Thia-3,4,8-triaza-benzo[de]cyclopenta[b]anthracen-7-one

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:133401-10-2 SDS

133401-10-2Downstream Products

133401-10-2Relevant articles and documents

Synthetic studies on pentacyclic aromatic alkaloids, kuanoniamine A, 11-hydroxyascididemin, and neocalliactine acetate

Kitahara, Yoshiyasu,Nakahara, Shinsuke,Yonezawa, Takanobu,Nagatsu, Masanori,Shibano, Yoshikazu,Kubo, Akinori

, p. 17029 - 17038 (2007/10/03)

A pentacyclic aromatic alkaloid, kuanoniamine A (6) was synthesized in three steps from 6-methoxybenzothiazole-4,7-dione (8) and 2-aminoacetophenone (9). 11-Hydroxyascididemin (4) was prepared from 5,8-quinolinedione (13, 14) or 1,4-acridinedione (20). The structure of neocalliactine acetate, a derivative of calliactine, was determined to be 5 by total synthesis from 6-methoxy-5,8-quinolinedione (28) and 2-amino-5-methoxyacetophenone (29).

Efficient and convenient pyridine ring-e formation of the cytotoxic marine alkaloid ascididemin and related analogues

Lindsay, Brent S.,Pearce, A. Norrie,Copp, Brent R.

, p. 2587 - 2592 (2007/10/03)

Abstract Conversion of tetracyclic quinone 1 to the cytotoxic pentacyclic alkaloid ascididemin (2) in 80% yield is achieved by reaction with paraformaldehyde and ammonium chloride in refluxing acetic acid. High yielding annelations are also observed for the related analogues N-8 deaza ascididemin (3) and kuanoniamine A (4).

TOTAL SYNTHESIS OF KUANONIAMINE A, 11-HYDROXYASCIDIDEMIN, AND NEOCALLIACTINE ACETATE

Kitahara, Yoshiyasu,Nakahara, Shinsuke,Yonezawa, Takanobu,Nagatsu, Masanori,Kubo, Akinori

, p. 943 - 946 (2007/10/02)

A pentacyclic aromatic alkaloid, kuanoniamine A (5) was synthesized from 6-methoxybenzothiazole-4,7-dione (7) and 2-aminoacetophenone (8).Similarly, 11-hydroxyascididemin (4) was prepared from 6-bromo-4-chloro-5,8-dimethoxyquinoline (12).The structure of neocalliactine acetate, a derivative of calliactine, was determined as 19 by total synthesis from 6-methoxy-5,8-quinolinedione (23) and 2-amino-5-methoxyacetophenone (24).

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