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phenyl [1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-ylmethyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 876885-74-4 Structure
  • Basic information

    1. Product Name: phenyl [1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-ylmethyl ether
    2. Synonyms: phenyl [1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-ylmethyl ether;6-(phenoxymethyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole
    3. CAS NO:876885-74-4
    4. Molecular Formula: C10H8N4OS
    5. Molecular Weight: 232.26172
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 876885-74-4.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: phenyl [1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-ylmethyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl [1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-ylmethyl ether(876885-74-4)
    11. EPA Substance Registry System: phenyl [1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-ylmethyl ether(876885-74-4)
  • 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: 876885-74-4(Hazardous Substances Data)

876885-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876885-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,8,8 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 876885-74:
(8*8)+(7*7)+(6*6)+(5*8)+(4*8)+(3*5)+(2*7)+(1*4)=254
254 % 10 = 4
So 876885-74-4 is a valid CAS Registry Number.

876885-74-4Downstream Products

876885-74-4Relevant articles and documents

Utilization of 2-halo-1,3,4-thiadiazoles in the synthesis of 2-functionalized 1,3,4-thiadiazole derivatives

Wang, Xi-Cun,Luo, Jin-Ge,Ding, Xiao-Mei,Quan, Zheng-Jun

, p. 2275 - 2287 (2011/11/06)

Novel 2-bromo/iodo-5-aryloxymethyl-1,3,4-thiadiazoles were prepared by the diazotization of 2-amino-1,3,4-thiadiazoles using p-TsOH as acid under the copper-free conditions. 2-Chloro-5-aryloxymethyl- 1,3,4-thiadiazoles, which were prepared by traditional

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