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CAS

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1312791-17-5

(R)-2-(4-Nitrophenyl)-5-(trimethylsilyl)pent-4-yn-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1312791-17-5 Structure

  • Basic information

    1. Product Name: (R)-2-(4-Nitrophenyl)-5-(trimethylsilyl)pent-4-yn-2-ol
    2. Synonyms: (R)-2-(4-Nitrophenyl)-5-(trimethylsilyl)pent-4-yn-2-ol
    3. CAS NO:1312791-17-5
    4. Molecular Formula:
    5. Molecular Weight: 277.395
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1312791-17-5.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: (R)-2-(4-Nitrophenyl)-5-(trimethylsilyl)pent-4-yn-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-(4-Nitrophenyl)-5-(trimethylsilyl)pent-4-yn-2-ol(1312791-17-5)
    11. EPA Substance Registry System: (R)-2-(4-Nitrophenyl)-5-(trimethylsilyl)pent-4-yn-2-ol(1312791-17-5)

  • 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: 1312791-17-5(Hazardous Substances Data)

1312791-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1312791-17-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,7,9 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1312791-17:
(9*1)+(8*3)+(7*1)+(6*2)+(5*7)+(4*9)+(3*1)+(2*1)+(1*7)=135
135 % 10 = 5
So 1312791-17-5 is a valid CAS Registry Number.

1312791-17-5Downstream Products

1312791-17-5Relevant articles and documents

A general copper-BINAP-catalyzed asymmetric propargylation of ketones with propargyl boronates

Fandrick, Keith R.,Fandrick, Daniel R.,Reeves, Jonathan T.,Gao, Joe,Ma, Shengli,Li, Wenjie,Lee, Heewon,Grinberg, Nelu,Lu, Bruce,Senanayake, Chris H.

supporting information; experimental part, p. 10332 - 10335 (2011/09/13)

An operationally simple copper-BINAP-catalyzed, highly enantioselective propargylation of ketones is presented. The methodology was developed as an enantioselective process for methyl ethyl ketone and shown to be applicable to a wide variety of prochiral

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