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167905-70-6

(6-(4-methylbenzoyl)-2-oxo-1,3-benzothiazol-3-yl)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 167905-70-6 Structure

  • Basic information

    1. Product Name: (6-(4-methylbenzoyl)-2-oxo-1,3-benzothiazol-3-yl)acetic acid
    2. Synonyms:
    3. CAS NO:167905-70-6
    4. Molecular Formula:
    5. Molecular Weight: 327.361
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 167905-70-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (6-(4-methylbenzoyl)-2-oxo-1,3-benzothiazol-3-yl)acetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (6-(4-methylbenzoyl)-2-oxo-1,3-benzothiazol-3-yl)acetic acid(167905-70-6)
    11. EPA Substance Registry System: (6-(4-methylbenzoyl)-2-oxo-1,3-benzothiazol-3-yl)acetic acid(167905-70-6)

  • 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: 167905-70-6(Hazardous Substances Data)

167905-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167905-70-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,9,0 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 167905-70:
(8*1)+(7*6)+(6*7)+(5*9)+(4*0)+(3*5)+(2*7)+(1*0)=166
166 % 10 = 6
So 167905-70-6 is a valid CAS Registry Number.

167905-70-6Upstream product

167905-70-6Downstream Products

167905-70-6Relevant articles and documents

Microwave-assisted synthesis of 1,3-benzothiazol-2(3 H)-one derivatives and analysis of their antinociceptive activity

?nkol,Dündar,Yldrm,Erol,?ahin

, p. 571 - 575 (2012)

A rapid and efficient method was developed for synthesis of 6-acyl-1,3-benzothiazol-2(3H)-one derivatives under microwave irradiation (MWI) conditions. The reaction times were shortened compared to conventional heating. Additionally, we synthesized acetic acid and acetamide derivatives of 1,3-benzothiazol-2(3H)-one, 6-acyl-1,3-benzothiazol-2(3H)-one, 5-chloro-1,3-benzothiazol-2(3H)-one and 6-acyl-5-chloro-1,3-benzothiazol-2(3H)- one with the microwave-assisted method and analyzed their antinociceptive activity with the tail flick, tail clip, hot plate and writhing tests. Among the synthesized compounds, 3-[2-(4-ethylpiperazin-1-yl)-2-oxoethyl]-1,3- benzothiazol-2(3H)-one (6a), 5-chloro-3-{2-oxo-2-[4-(propan-2-yl) piperazin-1-yl]ethyl}-1,3-benzothiazol-2(3H)-one (7e) and 3-[2-(4- butylpiperazin-1-yl)-2-oxoethyl]-5-chloro-1,3-benzothiazol-2(3H)-one (8e) showed significant antinociceptive activity in the tail clip, tail flick, hot plate and writhing tests. Supporting Information available online at http://www.thieme-connect.de/ejournals/toc/amf.

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