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CAS

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140629-82-9

3-<(1S,6R)-6-((S)-p-tolylsulfinyl)bicyclo<4.1.0>hept-1-yl>prop-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 140629-82-9 Structure

  • Basic information

    1. Product Name: 3-<(1S,6R)-6-((S)-p-tolylsulfinyl)bicyclo<4.1.0>hept-1-yl>prop-1-ene
    2. Synonyms: 3-<(1S,6R)-6-((S)-p-tolylsulfinyl)bicyclo<4.1.0>hept-1-yl>prop-1-ene
    3. CAS NO:140629-82-9
    4. Molecular Formula:
    5. Molecular Weight: 274.427
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 140629-82-9.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: 3-<(1S,6R)-6-((S)-p-tolylsulfinyl)bicyclo<4.1.0>hept-1-yl>prop-1-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-<(1S,6R)-6-((S)-p-tolylsulfinyl)bicyclo<4.1.0>hept-1-yl>prop-1-ene(140629-82-9)
    11. EPA Substance Registry System: 3-<(1S,6R)-6-((S)-p-tolylsulfinyl)bicyclo<4.1.0>hept-1-yl>prop-1-ene(140629-82-9)

  • 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: 140629-82-9(Hazardous Substances Data)

140629-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140629-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,2 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 140629-82:
(8*1)+(7*4)+(6*0)+(5*6)+(4*2)+(3*9)+(2*8)+(1*2)=119
119 % 10 = 9
So 140629-82-9 is a valid CAS Registry Number.

140629-82-9Relevant articles and documents

Asymmetric cyclopropanation by reaction of a γ-chloromethylated chiral vinylic sulfoxide with allylmagnesium bromide

Takemoto,Ohra,Sugiyama,Imanishi,Iwata

, p. 571 - 577 (2007/10/02)

An optically active vinylic sulfoxide bearing a leaving group at the γ-position was stereoselectively transformed into a chiral cyclopropane by means of a Michael addition with an allylmagnesinm bromide. The Michael induced ring-closure reaction requires both allylmagnesium bromide as a nucleophile and chloride as a leaving group for high diastereoselectivity. The absolute stereochemistry of the cycloadduct was confirmed by X-ray analysis.

Novel Asymmetric Cyclopropanation Utilizing Sulfinyl Chirality: Application to Construction of a Spirodecane System

Imanishi, Takeshi,Ohra, Taiichi,Sugiyama, Kenji,Ueda, Yoko,Takemoto, Yoshiji,Iwata, Chuzo

, p. 269 - 270 (2007/10/02)

An optically active vinylic sulfoxide is stereoselectively transformed into a chiral cyclopropane by means of a Michael addition reaction with an allyl Grignard reagent, and using this novel cyclopropanation, asymmetric construction of a spirodecane

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