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CAS

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1610462-00-4

(1S,2R)-2-(2,3-dimethylphenyl)-1,2-dihydronaphthalen-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1610462-00-4 Structure

  • Basic information

    1. Product Name: (1S,2R)-2-(2,3-dimethylphenyl)-1,2-dihydronaphthalen-1-ol
    2. Synonyms:
    3. CAS NO:1610462-00-4
    4. Molecular Formula:
    5. Molecular Weight: 250.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1610462-00-4.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: (1S,2R)-2-(2,3-dimethylphenyl)-1,2-dihydronaphthalen-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,2R)-2-(2,3-dimethylphenyl)-1,2-dihydronaphthalen-1-ol(1610462-00-4)
    11. EPA Substance Registry System: (1S,2R)-2-(2,3-dimethylphenyl)-1,2-dihydronaphthalen-1-ol(1610462-00-4)

  • 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: 1610462-00-4(Hazardous Substances Data)

1610462-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610462-00-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,4,6 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1610462-00:
(9*1)+(8*6)+(7*1)+(6*0)+(5*4)+(4*6)+(3*2)+(2*0)+(1*0)=114
114 % 10 = 4
So 1610462-00-4 is a valid CAS Registry Number.

1610462-00-4Downstream Products

1610462-00-4Relevant articles and documents

Nickel-catalyzed asymmetric ring opening of oxabenzonorbornadienes with arylboronic acids

Zeng, Zhongyi,Yang, Dingqiao,Long, Yuhua,Pan, Xuejing,Huang, Guobao,Zuo, Xiongjun,Zhou, Wen

, p. 5249 - 5257 (2014/06/23)

A new, versatile, and highly efficient nickel-catalyzed asymmetric ring-opening (ARO) reaction of oxabenzonorbornadienes with a wide variety of arylboronic acids has been developed, yielding cis-2-aryl-1,2-dihydronaphthalen- 1-ols in high yields (up to 99%) with good to excellent enantioselectivities (up to 99% ee) under very mild conditions. The effects of various nickel precursors, chiral bidentate ligands, catalyst loadings, bases, solvents, and temperatures on the yield and enantioselectivity of the reaction were also investigated. A plausible mechanism was proposed to account for the formation of the corresponding cis-ring-opened products based on the X-ray structure of product 4b.

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