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CAS

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219773-69-0

6,7-DIMETHOXY-2-(2-THIENYL)-4H-3,1-BENZOXAZIN-4-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 219773-69-0 Structure

  • Basic information

    1. Product Name: 6,7-DIMETHOXY-2-(2-THIENYL)-4H-3,1-BENZOXAZIN-4-ONE
    2. Synonyms: 6,7-DIMETHOXY-2-(2-THIENYL)-4H-3,1-BENZOXAZIN-4-ONE
    3. CAS NO:219773-69-0
    4. Molecular Formula: C14H11NO4S
    5. Molecular Weight: 289.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 219773-69-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6,7-DIMETHOXY-2-(2-THIENYL)-4H-3,1-BENZOXAZIN-4-ONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,7-DIMETHOXY-2-(2-THIENYL)-4H-3,1-BENZOXAZIN-4-ONE(219773-69-0)
    11. EPA Substance Registry System: 6,7-DIMETHOXY-2-(2-THIENYL)-4H-3,1-BENZOXAZIN-4-ONE(219773-69-0)

  • 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: 219773-69-0(Hazardous Substances Data)

219773-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219773-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,7,7 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 219773-69:
(8*2)+(7*1)+(6*9)+(5*7)+(4*7)+(3*3)+(2*6)+(1*9)=170
170 % 10 = 0
So 219773-69-0 is a valid CAS Registry Number.

219773-69-0Relevant articles and documents

The design and synthesis of novel orally active inhibitors of AP-1 and NF-κB mediated transcriptional activation. SAR of in vitro and in vivo studies

Palanki, Moorthy S. S.,Erdman, Paul E.,Ren, Minghuan,Suto, Mark,Bennett, Brydon L.,Manning, Anthony,Ransone, Lynn,Spooner, Cheryl,Desai, Sonal,Ow, Arnie,Totsuka, Ryuichi,Tsao, Peter,Toriumi, Wataru

, p. 4077 - 4080 (2007/10/03)

We have developed novel orally active quinazoline analogues as inhibitors of AP-1 and NF-κB mediated transcriptional activation. Among the derivatives prepared, 1-[2-(2-thienyl)quinazolin-4-ylamino]-3-methyl-3- pyrroline-2,5-dione (10) showed significant activity in an adjuvant-induced arthritis rat model by reducing the swelling by 65% in the non-injected foot. The synthesis, structure-activity relationship, and in vivo activity are described.

Quinazoline analogs and related compounds and methods for treating inflammatory conditions

-

, (2008/06/13)

Compounds having utility as anti-inflammatory agents in general and, more specifically, for the prevention and/or treatment of immunoinflammatory and autoimmune diseases are disclosed. The compounds are quinazoline-containing compounds. Methods are also d

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