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1386383-66-9

trimethyl[4-(3-nitrophenoxy)but-2-enyl]silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1386383-66-9 Structure

  • Basic information

    1. Product Name: trimethyl[4-(3-nitrophenoxy)but-2-enyl]silane
    2. Synonyms:
    3. CAS NO:1386383-66-9
    4. Molecular Formula:
    5. Molecular Weight: 265.384
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1386383-66-9.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: trimethyl[4-(3-nitrophenoxy)but-2-enyl]silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: trimethyl[4-(3-nitrophenoxy)but-2-enyl]silane(1386383-66-9)
    11. EPA Substance Registry System: trimethyl[4-(3-nitrophenoxy)but-2-enyl]silane(1386383-66-9)

  • 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: 1386383-66-9(Hazardous Substances Data)

1386383-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1386383-66-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,6,3,8 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1386383-66:
(9*1)+(8*3)+(7*8)+(6*6)+(5*3)+(4*8)+(3*3)+(2*6)+(1*6)=199
199 % 10 = 9
So 1386383-66-9 is a valid CAS Registry Number.

1386383-66-9Downstream Products

1386383-66-9Relevant articles and documents

Chiral 6-NHC ligand and copper complex: Properties, application, and mechanism

Park, Jinkyoon,McQuade, D.Tyler

, p. 1485 - 1490 (2012)

We demonstrated the synthesis of chiral annulated six-membered-ring N-heterocyclic carbenes (6-NHC) and their adducts with water and alcohol. We also have shown the donating properties of chiral annulated 6-NHCs is between that of typical 5-NHCs and 6-NHCs. We have shown the synthetic conditions for 6-NHC-copper complex formation. Using the chiral 6-NHC-copper complex, we synthesized unsaturated chiral bimetallic allylic boronate reagents with high enantioselectivity. Finally, we propose a catalytic cycle that justifies observed reactivity and provides a new explanation for the role methanol has in the reaction cycle; our cycle is supported by a primary kinetic isotope effect.

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