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CAS

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624744-96-3

7-Oxabicyclo[4.1.0]heptan-2-ol, 6-(2-propenyl)-, (1R,2R,6R)-rel- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 7-Oxabicyclo[4.1.0]heptan-2-ol, 6-(2-propenyl)-, (1R,2R,6R)-rel- (9CI)

    Cas No: 624744-96-3

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  • 624744-96-3 Structure

  • Basic information

    1. Product Name: 7-Oxabicyclo[4.1.0]heptan-2-ol, 6-(2-propenyl)-, (1R,2R,6R)-rel- (9CI)
    2. Synonyms: 7-Oxabicyclo[4.1.0]heptan-2-ol, 6-(2-propenyl)-, (1R,2R,6R)-rel- (9CI)
    3. CAS NO:624744-96-3
    4. Molecular Formula: C9H14O2
    5. Molecular Weight: 154.20626
    6. EINECS: N/A
    7. Product Categories: ALCOHOL
    8. Mol File: 624744-96-3.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: 7-Oxabicyclo[4.1.0]heptan-2-ol, 6-(2-propenyl)-, (1R,2R,6R)-rel- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Oxabicyclo[4.1.0]heptan-2-ol, 6-(2-propenyl)-, (1R,2R,6R)-rel- (9CI)(624744-96-3)
    11. EPA Substance Registry System: 7-Oxabicyclo[4.1.0]heptan-2-ol, 6-(2-propenyl)-, (1R,2R,6R)-rel- (9CI)(624744-96-3)

  • 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: 624744-96-3(Hazardous Substances Data)

624744-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 624744-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,4,7,4 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 624744-96:
(8*6)+(7*2)+(6*4)+(5*7)+(4*4)+(3*4)+(2*9)+(1*6)=173
173 % 10 = 3
So 624744-96-3 is a valid CAS Registry Number.

624744-96-3Upstream product

624744-96-3Downstream Products

624744-96-3Relevant articles and documents

Progressive studies on the novel samarium-catalyzed diastereoselective tandem semipinacol rearrangement/Tishchenko reduction of secondary α-hydroxy epoxides

Fan, Chun-An,Hu, Xiang-Dong,Tu, Yong-Qiang,Wang, Bao-Min,Song, Zhen-Lei

, p. 4301 - 4310 (2003)

A novel and highly diastereoselective samarium-catalyzed tandem rearrangement/reduction of secondary a-hydroxy epoxides, which involves a C1 to C3 carbon migration rearrangement and a very interesting hetero-Tishchenko reduction of the intermediate aldehy

Indium-promoted chemo- and diastereoselective allylation of α,β-epoxy ketones with potassium allyltrifluoroborate

Nowrouzi, Farhad,Janetzko, John,Batey, Robert A.

supporting information; experimental part, p. 5490 - 5493 (2011/02/27)

A practical method for the chemo- and diastereoselective allylation of α,β-epoxy ketones has been developed by using the convenient air and moisture stable reagent potassium allyltrifluoroborate. Indium metal was found to promote addition in stoichiometric or catalytic amounts, to afford α,β-epoxyhomoallylic tertiary alcohols in high yields and diastereoselectivities, without competing ring-scission of the epoxide.

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