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CAS

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501948-05-6

3-[(4-Cyanophenyl)methyl]-N-(3-methyl-5-isothiazolyl)-alpha-oxo-1-indolizineacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1-Indolizineacetamide,3-[(4-cyanophenyl)methyl]-N-(3-methyl-5-isothiazolyl)-a-oxo-

    Cas No: 501948-05-6

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  • 501948-05-6 Structure

  • Basic information

    1. Product Name: 3-[(4-Cyanophenyl)methyl]-N-(3-methyl-5-isothiazolyl)-alpha-oxo-1-indolizineacetamide
    2. Synonyms: 3-[(4-Cyanophenyl)methyl]-N-(3-methyl-5-isothiazolyl)-alpha-oxo-1-indolizineacetamide;Rosabulin;STA 5312
    3. CAS NO:501948-05-6
    4. Molecular Formula: C22H16N4O2S
    5. Molecular Weight: 400.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 501948-05-6.mol

  • Chemical Properties

    1. Melting Point: 233 ºC
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.34
    6. Refractive Index: 1.7
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.00±0.46(Predicted)
    10. CAS DataBase Reference: 3-[(4-Cyanophenyl)methyl]-N-(3-methyl-5-isothiazolyl)-alpha-oxo-1-indolizineacetamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-[(4-Cyanophenyl)methyl]-N-(3-methyl-5-isothiazolyl)-alpha-oxo-1-indolizineacetamide(501948-05-6)
    12. EPA Substance Registry System: 3-[(4-Cyanophenyl)methyl]-N-(3-methyl-5-isothiazolyl)-alpha-oxo-1-indolizineacetamide(501948-05-6)

  • 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: 501948-05-6(Hazardous Substances Data)

501948-05-6 Usage

Uses

Treatment of therapeutic resistant cancers.

Check Digit Verification of cas no

The CAS Registry Mumber 501948-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,9,4 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 501948-05:
(8*5)+(7*0)+(6*1)+(5*9)+(4*4)+(3*8)+(2*0)+(1*5)=136
136 % 10 = 6
So 501948-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H16N4O2S/c1-14-10-20(29-25-14)24-22(28)21(27)18-12-17(26-9-3-2-4-19(18)26)11-15-5-7-16(13-23)8-6-15/h2-10,12H,11H2,1H3,(H,24,28)

501948-05-6SDS

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 2-[3-[(4-cyanophenyl)methyl]indolizin-1-yl]-N-(3-methyl-1,2-thiazol-5-yl)-2-oxoacetamide

1.2 Other means of identification

Product number -
Other names UNII-6Z674O12T6

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:501948-05-6 SDS

501948-05-6Downstream Products

501948-05-6Relevant articles and documents

Development of a practical synthesis of STA-5312, a novel indolizine oxalylamide microtubule inhibitor

Li, Hao,Xia, Zhiqiang,Chen, Shoujun,Koya, Keizo,Ono, Mitsunori,Sun, Lijun

, p. 246 - 250 (2007)

An efficient synthesis of the novel microtubule inhibitor STA-5312(3-[(4-cyanophenyl)methyl]-N-3-methyl-5-isothiazolyl) -α-oxo-1-indolizineacetamide) was developed. A novel DMF/ Me 2SO4 directed regioselective synthesis of the 3-(4-c

Indolizine compounds

-

, (2008/06/13)

This invention relates to compounds of Formula (I) wherein Ring A, X, Y, Z, R1, R2 and R3 are defined herein. These compounds are useful for treating and preventing cancer, inflammatory disorders, autoimmune diseases and o

1-Glyoxlylamide indolizines for treating cancer

-

, (2008/06/13)

Disclosed is a compound represented by Structural Formula (I): Ring A is substituted or unsubstituted and optionally fused to an aryl group. Z1 and Z2 are independently ═O, ═S, ═N—OR12 or ═NR12 R1 an

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