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CAS

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127311-30-2

(1R*,2S*,3R*)-6-hydroxy-1-(4-hydroxyphenyl)-2,5,7-trimethyl-3-(2-phenylethyl)-2,3-dihydroindene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127311-30-2 Structure

  • Basic information

    1. Product Name: (1R*,2S*,3R*)-6-hydroxy-1-(4-hydroxyphenyl)-2,5,7-trimethyl-3-(2-phenylethyl)-2,3-dihydroindene
    2. Synonyms:
    3. CAS NO:127311-30-2
    4. Molecular Formula:
    5. Molecular Weight: 372.507
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127311-30-2.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: (1R*,2S*,3R*)-6-hydroxy-1-(4-hydroxyphenyl)-2,5,7-trimethyl-3-(2-phenylethyl)-2,3-dihydroindene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R*,2S*,3R*)-6-hydroxy-1-(4-hydroxyphenyl)-2,5,7-trimethyl-3-(2-phenylethyl)-2,3-dihydroindene(127311-30-2)
    11. EPA Substance Registry System: (1R*,2S*,3R*)-6-hydroxy-1-(4-hydroxyphenyl)-2,5,7-trimethyl-3-(2-phenylethyl)-2,3-dihydroindene(127311-30-2)

  • 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: 127311-30-2(Hazardous Substances Data)

127311-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127311-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,3,1 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127311-30:
(8*1)+(7*2)+(6*7)+(5*3)+(4*1)+(3*1)+(2*3)+(1*0)=92
92 % 10 = 2
So 127311-30-2 is a valid CAS Registry Number.

127311-30-2Downstream Products

127311-30-2Relevant articles and documents

Formal Cycloaddition of Benzylic Cations with Alkenes

Angle, Steven R.,Arnaiz, Damian O.

, p. 5937 - 5947 (2007/10/02)

The reaction of benzylic cations with styrenes affords dihydro(1H)indenes in good yield via a formal atom cycloadditon.The cations were generated from quinone methides and benzylic alcohols. (E)-Styrenes participate in the reaction with remarkable stereoselectivity affording dihydro(1H)indenes with three stereogenic centers with >40:1 diastereoselectivity.A possible transition state for the reaction is discussed.Less activated alkenes such as dihydropyran and methylcyclohexane afforded cycloadducts in 66percent and 51percent yields, respectively.

Synthesis of Dihydro-1H-indenes via a Formal 3 + 2 Cycloaddition of p-Quinone Methides and Styrenes

Angle, Steven R.,Arnaiz, Damian O.

, p. 3708 - 3710 (2007/10/02)

The synthesis of dihydro-1H-indenes via the formal 3 + 2 cycloaddition of an electron-rich alkene and a p-quinone methide is reported.

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