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1254100-04-3

4-(2,2-dioxido-3,4,7,8-tetrahydro-6H-pyrrolo[2,1-c][1,2,4,6]thiatriazin-4-yl)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1254100-04-3 Structure

  • Basic information

    1. Product Name: 4-(2,2-dioxido-3,4,7,8-tetrahydro-6H-pyrrolo[2,1-c][1,2,4,6]thiatriazin-4-yl)benzoic acid
    2. Synonyms:
    3. CAS NO:1254100-04-3
    4. Molecular Formula:
    5. Molecular Weight: 295.319
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1254100-04-3.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: 4-(2,2-dioxido-3,4,7,8-tetrahydro-6H-pyrrolo[2,1-c][1,2,4,6]thiatriazin-4-yl)benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(2,2-dioxido-3,4,7,8-tetrahydro-6H-pyrrolo[2,1-c][1,2,4,6]thiatriazin-4-yl)benzoic acid(1254100-04-3)
    11. EPA Substance Registry System: 4-(2,2-dioxido-3,4,7,8-tetrahydro-6H-pyrrolo[2,1-c][1,2,4,6]thiatriazin-4-yl)benzoic acid(1254100-04-3)

  • 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: 1254100-04-3(Hazardous Substances Data)

1254100-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1254100-04-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,1,0 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1254100-04:
(9*1)+(8*2)+(7*5)+(6*4)+(5*1)+(4*0)+(3*0)+(2*0)+(1*4)=93
93 % 10 = 3
So 1254100-04-3 is a valid CAS Registry Number.

1254100-04-3Downstream Products

1254100-04-3Relevant articles and documents

A facile synthesis of annulated thiatriazine dioxides

Khodachenko, Alexander N.,Shivanyuk, Alexander N.,Shishkina, Svetlana V.,Shishkin, Oleg V.,Nazarenko, Konstantin G.,Tolmachev, Andrey A.

experimental part, p. 2588 - 2598 (2010/09/05)

The reactions of five-, six-, seven-, and eight-membered cyclic imido ethers with one equivalent of sulfamide lead to the corresponding sulfamoylamidines in 70-80% yields. Sulfamoylamidines undergo condensations with aliphatic and aromatic aldehydes as well as aliphatic ketones to give thiatriazine dioxides in 50-95% yields. The NMR spectroscopic studies reveal ring-chain tautomerism of some thiatriazine dioxides in solution. The ratio between the tautomers depends on the temperature, solvent polarity, and electronic properties of the substituents of the pendant aryl rings. Thiatriazine dioxides are readily alkylated and acylated at position 2. Georg Thieme Verlag Stuttgart New York.

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