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133625-61-3

3H-Benzofuro[3,2-c]pyrazole, 3a,8-bta--dihydro- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133625-61-3 Structure

  • Basic information

    1. Product Name: 3H-Benzofuro[3,2-c]pyrazole, 3a,8-bta--dihydro- (9CI)
    2. Synonyms: 3H-Benzofuro[3,2-c]pyrazole, 3a,8-bta--dihydro- (9CI)
    3. CAS NO:133625-61-3
    4. Molecular Formula: C9H8N2O
    5. Molecular Weight: 160.17262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133625-61-3.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: 3H-Benzofuro[3,2-c]pyrazole, 3a,8-bta--dihydro- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3H-Benzofuro[3,2-c]pyrazole, 3a,8-bta--dihydro- (9CI)(133625-61-3)
    11. EPA Substance Registry System: 3H-Benzofuro[3,2-c]pyrazole, 3a,8-bta--dihydro- (9CI)(133625-61-3)

  • 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: 133625-61-3(Hazardous Substances Data)

133625-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133625-61-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,2 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 133625-61:
(8*1)+(7*3)+(6*3)+(5*6)+(4*2)+(3*5)+(2*6)+(1*1)=113
113 % 10 = 3
So 133625-61-3 is a valid CAS Registry Number.

133625-61-3Downstream Products

133625-61-3Relevant articles and documents

Intramolecular addition reactions of functionalized arylcarbenes to double bonds

Kirmse, Wolfgang,H?mberger, Günter

, p. 3925 - 3934 (2007/10/02)

Arylcarbenes with unsaturated ortho substituents (vinyloxy, 1-propenyloxy, allyl, 2-butenyl, 2,4-pentadienyl) were generated in methanol by photolysis of diazo precursors. Intermolecular OH insertion was found to compete with intramolecular addition to th

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