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1610862-99-1

1-deuteromethoxy-3,5-dimethoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1610862-99-1 Structure

  • Basic information

    1. Product Name: 1-deuteromethoxy-3,5-dimethoxybenzene
    2. Synonyms: 1-deuteromethoxy-3,5-dimethoxybenzene
    3. CAS NO:1610862-99-1
    4. Molecular Formula:
    5. Molecular Weight: 171.169
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1610862-99-1.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-deuteromethoxy-3,5-dimethoxybenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-deuteromethoxy-3,5-dimethoxybenzene(1610862-99-1)
    11. EPA Substance Registry System: 1-deuteromethoxy-3,5-dimethoxybenzene(1610862-99-1)

  • 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: 1610862-99-1(Hazardous Substances Data)

1610862-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610862-99-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,8,6 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1610862-99:
(9*1)+(8*6)+(7*1)+(6*0)+(5*8)+(4*6)+(3*2)+(2*9)+(1*9)=161
161 % 10 = 1
So 1610862-99-1 is a valid CAS Registry Number.

1610862-99-1Upstream product

1610862-99-1Downstream Products

1610862-99-1Relevant articles and documents

Palladium-catalyzed methoxylation of aromatic chlorides with borate salts

Tolnai, Gergely L.,Petho, Bálint,Králl, Péter,Nováka, Zoltán

, p. 125 - 129 (2014)

Herein we disclose a simple palladiumcatalyzed transformation for the methoxylation of aromatic chlorides with tetramethoxyborate salts. The procedure provides a new and efficient synthetic tool for the introduction of a methoxy group into aromatic systems. In addition, the reaction can be achieved using a wide range of aromatic and heteroaromatic chlorides, the cheapest class of halides.

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