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CAS

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1379659-20-7

N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-methoxy-furazan-3-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1379659-20-7 Structure

  • Basic information

    1. Product Name: N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-methoxy-furazan-3-amine
    2. Synonyms:
    3. CAS NO:1379659-20-7
    4. Molecular Formula:
    5. Molecular Weight: 235.165
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1379659-20-7.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: N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-methoxy-furazan-3-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-methoxy-furazan-3-amine(1379659-20-7)
    11. EPA Substance Registry System: N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-methoxy-furazan-3-amine(1379659-20-7)

  • 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: 1379659-20-7(Hazardous Substances Data)

1379659-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379659-20-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,6,5 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1379659-20:
(9*1)+(8*3)+(7*7)+(6*9)+(5*6)+(4*5)+(3*9)+(2*2)+(1*0)=217
217 % 10 = 7
So 1379659-20-7 is a valid CAS Registry Number.

1379659-20-7Downstream Products

1379659-20-7Relevant articles and documents

A Direct approach to a 6-hetarylamino[1,2,4]triazolo[4,3-b][1,2,4,5] tetrazine library

Palysaeva, Nadezhda V.,Kumpan, Katerina P.,Struchkova, Marina I.,Dalinger, Igor L.,Kormanov, Aleksandr V.,Aleksandrova, Nataly S.,Chernyshev, Victor M.,Pyreu, Dmitrii F.,Suponitsky, Kyrill Yu.,Sheremetev, Aleksei B.

supporting information, p. 406 - 409 (2014/04/03)

The synthesis of 6-hetarylamino[1,2,4]triazolo[4,3-b]-[1,2,4,5]tetrazines is reported. The functionalized secondary amines were constructed via a K 2CO3-mediated SNAr reaction of weakly basic hetarylamines with 3-(3,5-dimethylpyrazol-1-yl)[1,2,4]triazolo[4,3-b]-[1,2,4,5]tetrazines, which allowed displacement 3,5-dimethylpyrazolyl leaving group. Significantly, the reaction exhibited a broad substrate scope and proceeded in good yields.

Copper-catalyzed C-N coupling reactions of nitrogen-rich compounds - Reaction of iodofurazans with s-tetrazinylamines

Sheremetev, Aleksei B.,Palysaeva, Nadezhda V.,Struchkova, Marina I.,Suponitsky, Kyrill Yu.,Antipin, Mikhail Yu.

experimental part, p. 2266 - 2272 (2012/06/15)

Access to unsymmetrical secondary dihetarylamines through the Cu(OAc) 2/2-acetylcyclohexanone catalyzed cross-coupling of s-tetrazinylamines with iodofurazans has been developed. The reaction displays good functional group tolerance, involving

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