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1034138-03-8

1-phenylnon-4-yn-3-yl methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1034138-03-8 Structure

  • Basic information

    1. Product Name: 1-phenylnon-4-yn-3-yl methanesulfonate
    2. Synonyms: 1-phenylnon-4-yn-3-yl methanesulfonate
    3. CAS NO:1034138-03-8
    4. Molecular Formula:
    5. Molecular Weight: 294.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1034138-03-8.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-phenylnon-4-yn-3-yl methanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenylnon-4-yn-3-yl methanesulfonate(1034138-03-8)
    11. EPA Substance Registry System: 1-phenylnon-4-yn-3-yl methanesulfonate(1034138-03-8)

  • 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: 1034138-03-8(Hazardous Substances Data)

1034138-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034138-03-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,1,3 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1034138-03:
(9*1)+(8*0)+(7*3)+(6*4)+(5*1)+(4*3)+(3*8)+(2*0)+(1*3)=98
98 % 10 = 8
So 1034138-03-8 is a valid CAS Registry Number.

1034138-03-8Relevant articles and documents

Spirodiepoxide-based cascades: Direct access to diverse motifs

Sharma, Rojita,Manpadi, Madhuri,Zhang, Yue,Kim, Hiyun,Ahkmedov, Novruz G.,Williams, Lawrence J.

supporting information; experimental part, p. 3352 - 3355 (2011/08/22)

Allene epoxide formation/opening reaction sequences enabled direct access to diverse products. Described here are a single flask procedure for allene preparation and allene oxidation/derivatization reactions that give, among others, diendiol, diyndiol, α′-hydroxy-γ-enone, dihydrofuranone, butenolide, and δ-lactone products.

Stereospecific anti SE2′ fluorination of allenylsilanes: Synthesis of enantioenriched propargylic fluorides

Carroll, Laurence,McCullough, Samantha,Rees, Tom,Claridge, Timothy D. W.,Gouverneur, Veronique

supporting information; experimental part, p. 1731 - 1733 (2008/10/09)

The electrophilic fluorodesilylation of enantioenriched allenylsilanes proceeds with efficient transfer of chirality. The silylation-fluorination of propargylic alcohols occurs with overall retention of stereochemistry, a result consistent with a stereosp

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