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5H,7H-Imidazo[1,2-c]thiazole-2-carboxaldehyde (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 623564-72-7 Structure
  • Basic information

    1. Product Name: 5H,7H-Imidazo[1,2-c]thiazole-2-carboxaldehyde (9CI)
    2. Synonyms: 5H,7H-Imidazo[1,2-c]thiazole-2-carboxaldehyde (9CI);5H,7H-Imidazo[1,2-c]thiazole-2-carboxaldehyde
    3. CAS NO:623564-72-7
    4. Molecular Formula: C6H6N2OS
    5. Molecular Weight: 154.18964
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY;ALDEHYDE
    8. Mol File: 623564-72-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 436.3±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.55±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.05±0.20(Predicted)
    10. CAS DataBase Reference: 5H,7H-Imidazo[1,2-c]thiazole-2-carboxaldehyde (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5H,7H-Imidazo[1,2-c]thiazole-2-carboxaldehyde (9CI)(623564-72-7)
    12. EPA Substance Registry System: 5H,7H-Imidazo[1,2-c]thiazole-2-carboxaldehyde (9CI)(623564-72-7)
  • 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: 623564-72-7(Hazardous Substances Data)

623564-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 623564-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,5,6 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 623564-72:
(8*6)+(7*2)+(6*3)+(5*5)+(4*6)+(3*4)+(2*7)+(1*2)=157
157 % 10 = 7
So 623564-72-7 is a valid CAS Registry Number.

623564-72-7Downstream Products

623564-72-7Relevant articles and documents

Bicyclic 6-alkylidene-penems as class-D beta-lactamases inhibitors

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Page/Page column 24, (2010/11/25)

This invention relates to certain bicyclic 6-alkylidene penems which act as a inhibitor of class-D enzymes. β-Lactamases hydrolyze β-lactam antibiotics, and as such serve as the primary cause of bacterial resistance. The compounds of the present invention when combined with β-lactam antibiotics will provide an effective treatment against life threatening bacterial infections. In accordance with the present invention there are provided compounds of general formula I or a pharmaceutically acceptable salt or in vivo hydrolyzable ester R5 thereof: wherein: One of A and B denotes hydrogen and the other an optionally substituted fused bicyclic heteroaryl group; and X═O or S.

Process for preparing 6-alkylidene penem derivatives

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, (2008/06/13)

The present invention provides a process of making compounds of formula I, which are useful for the treatment of bacterial infection or disease.

BICYCLIC 6-ALKYLIDENE-PENEMS AS ?-LACTAMASES INHIBITORS

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Page/Page column 83, (2008/06/13)

The present invention provides a compound of Formula (I), pharmaceutical compositions and the use thereof for the treatment of bacterial infection or disease in a patient in need thereof.

PROCESS FOR PREPARING 6-ALKYLIDENE PENEM DERIVATIVES

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Page/Page column 110-111, (2010/02/07)

The present invention provides a process of making compounds of Formula (I), which are useful for the treatment of bacterial infection or disease.

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