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Benzene, 1,3-dimethoxy-5-[(2-propynyloxy)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 876366-16-4 Structure
  • Basic information

    1. Product Name: Benzene, 1,3-dimethoxy-5-[(2-propynyloxy)methyl]-
    2. Synonyms:
    3. CAS NO:876366-16-4
    4. Molecular Formula: C12H14O3
    5. Molecular Weight: 206.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 876366-16-4.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: Benzene, 1,3-dimethoxy-5-[(2-propynyloxy)methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1,3-dimethoxy-5-[(2-propynyloxy)methyl]-(876366-16-4)
    11. EPA Substance Registry System: Benzene, 1,3-dimethoxy-5-[(2-propynyloxy)methyl]-(876366-16-4)
  • 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: 876366-16-4(Hazardous Substances Data)

876366-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876366-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,3,6 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 876366-16:
(8*8)+(7*7)+(6*6)+(5*3)+(4*6)+(3*6)+(2*1)+(1*6)=214
214 % 10 = 4
So 876366-16-4 is a valid CAS Registry Number.

876366-16-4Relevant articles and documents

Enantioselective Palladium-Catalyzed Hydrophosphinylation of Allenes with Phosphine Oxides: Access to Chiral Allylic Phosphine Oxides

Wang, Jun,Yang, Zhiping

supporting information, p. 27288 - 27292 (2021/11/17)

A Pd-catalyzed hydrophosphinylation of alkyl and aryl-oxyallenes with phosphine oxides has been developed for the efficient and rapid construction of a family of chiral allylic phosphine oxides with a diverse range of functional groups. This methodology was further applied in the facile construction of chiral 2H-chromene and later stage functionalization of cholesterol.

Pd-Catalyzed Hydroamination of Alkoxyallenes with Azole Heterocycles: Examples and Mechanistic Proposal

Bernar, Ivan,Fiser, Béla,Blanco-Ania, Daniel,Gómez-Bengoa, Enrique,Rutjes, Floris P. J. T.

supporting information, p. 4211 - 4214 (2017/08/23)

Palladium-catalyzed regio- and enantioselective addition of azole heterocycles to alkoxyallenes was developed (up to 92% yields and up to 94% ee). DFT calculations suggest a new Pd(0)-driven mechanistic pathway proceeding through protonation of the Pd-coo

Synthesis of Fréchet type dendritic benzyl propargyl ether and Fréchet type triazole dendrimer

Lee, Jae Wook,Kim, Jung Hwan,Kim, Byung-Ku,Shin, Won Suk,Jin, Sung-Ho

, p. 894 - 900 (2007/10/03)

Fréchet type dendritic benzyl propargyl ethers were synthesized by the reaction of propargyl bromide with the corresponding Fréchet type dendritic benzyl alcohol. A propargyl focal point functionalized dendrons were applied for the construction of symmetr

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