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CAS

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886969-01-3

1-bromomethyl-2-prop-2-ynyloxy-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 886969-01-3 Structure

  • Basic information

    1. Product Name: 1-bromomethyl-2-prop-2-ynyloxy-benzene
    2. Synonyms: 1-bromomethyl-2-prop-2-ynyloxy-benzene
    3. CAS NO:886969-01-3
    4. Molecular Formula:
    5. Molecular Weight: 225.085
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 886969-01-3.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: 1-bromomethyl-2-prop-2-ynyloxy-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-bromomethyl-2-prop-2-ynyloxy-benzene(886969-01-3)
    11. EPA Substance Registry System: 1-bromomethyl-2-prop-2-ynyloxy-benzene(886969-01-3)

  • 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: 886969-01-3(Hazardous Substances Data)

886969-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 886969-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,9,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 886969-01:
(8*8)+(7*8)+(6*6)+(5*9)+(4*6)+(3*9)+(2*0)+(1*1)=253
253 % 10 = 3
So 886969-01-3 is a valid CAS Registry Number.

886969-01-3Relevant articles and documents

Cu(I)-Catalyzed cycloaddition of constrained azido-alkynes: Access to 12- to 17-membered monomeric triazolophanes incorporating furanoside rings

Ray, Ankur,Manoj,Bhadbhade, Mohan M.,Mukhopadhyay, Ranjan,Bhattacharjya, Anup

, p. 2775 - 2778 (2006)

A strained monomeric 12-membered triazolophane was formed by the Cu(I)-catalyzed intramolecular cycloaddition of an azide to an alkyne having a constrained tether incorporating an aromatic ring and a furanoside ring. Similar cycloadditions of azido-alkyne

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