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CAS

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478272-66-1

Spiro[cyclopentane-1,2-[7]oxabicyclo[4.1.0]heptane], (1S,6R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 478272-66-1 Structure

  • Basic information

    1. Product Name: Spiro[cyclopentane-1,2-[7]oxabicyclo[4.1.0]heptane], (1S,6R)- (9CI)
    2. Synonyms: Spiro[cyclopentane-1,2-[7]oxabicyclo[4.1.0]heptane], (1S,6R)- (9CI)
    3. CAS NO:478272-66-1
    4. Molecular Formula: C10H16O
    5. Molecular Weight: 152.23344
    6. EINECS: N/A
    7. Product Categories: CYCLOPENTANE
    8. Mol File: 478272-66-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Spiro[cyclopentane-1,2-[7]oxabicyclo[4.1.0]heptane], (1S,6R)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Spiro[cyclopentane-1,2-[7]oxabicyclo[4.1.0]heptane], (1S,6R)- (9CI)(478272-66-1)
    11. EPA Substance Registry System: Spiro[cyclopentane-1,2-[7]oxabicyclo[4.1.0]heptane], (1S,6R)- (9CI)(478272-66-1)

  • 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: 478272-66-1(Hazardous Substances Data)

478272-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478272-66-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,2,7 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 478272-66:
(8*4)+(7*7)+(6*8)+(5*2)+(4*7)+(3*2)+(2*6)+(1*6)=191
191 % 10 = 1
So 478272-66-1 is a valid CAS Registry Number.

478272-66-1Upstream product

478272-66-1Downstream Products

478272-66-1Relevant articles and documents

Fragmentation of nitrone triflates to 9-membered rings

Murphy, John A.,Mahesh, Mohan,McPheators, Gary,Vijaya Anand,McGuire, Thomas M.,Carlinga, Robert,Kennedy, Alan R.

, p. 3233 - 3236 (2008/02/11)

A new fragmentative rearrangement of nitrone derivatives to form 9-membered rings is reported. The fragmentations are triggered when nitrones are treated with triflic anhydride; a C-C bond antiperiplanar to the cleaving N-O bond is activated either by an oxygen lone pair or by an electron-rich aromatic ring. In the former case, further cyclization of the 9-membered intermediate leads to a rearranged condensed ring system, but when triggered by arenes, 9-membered ring amides are isolated.

Novel Catalytic Kinetic Resolution of Racemic Epoxides to Allylic Alcohols

Gayet, Arnaud,Bertilsson, Sophie,Andersson, Pher G.

, p. 3777 - 3779 (2007/10/03)

(Matrix Presented) The kinetic resolution of racemic epoxides via catalytic enantioselective rearrangement to allylic alcohols was investigated. Using the Li-salt of (1S,3R,4R)-3-(pyrrolidinyl)methyl-2-azabicyclo [2.2.1] heptane 1 as catalyst allowed both

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