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1268496-02-1

3-([1,1′-biphenyl]-4-ylmethyl)indolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 3-([1,1′-biphenyl]-4-ylmethyl)indolin-2-one

    Cas No: 1268496-02-1

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  • 1268496-02-1 Structure

  • Basic information

    1. Product Name: 3-([1,1′-biphenyl]-4-ylmethyl)indolin-2-one
    2. Synonyms: 3-([1,1′-biphenyl]-4-ylmethyl)indolin-2-one
    3. CAS NO:1268496-02-1
    4. Molecular Formula:
    5. Molecular Weight: 299.372
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268496-02-1.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-([1,1′-biphenyl]-4-ylmethyl)indolin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-([1,1′-biphenyl]-4-ylmethyl)indolin-2-one(1268496-02-1)
    11. EPA Substance Registry System: 3-([1,1′-biphenyl]-4-ylmethyl)indolin-2-one(1268496-02-1)

  • 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: 1268496-02-1(Hazardous Substances Data)

1268496-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268496-02-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,4,9 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1268496-02:
(9*1)+(8*2)+(7*6)+(6*8)+(5*4)+(4*9)+(3*6)+(2*0)+(1*2)=191
191 % 10 = 1
So 1268496-02-1 is a valid CAS Registry Number.

1268496-02-1Relevant articles and documents

Transition-Metal-Free C-H Hydroxylation of Carbonyl Compounds

Chaudhari, Moreshwar B.,Sutar, Yogesh,Malpathak, Shreyas,Hazra, Anirban,Gnanaprakasam, Boopathy

, p. 3628 - 3631 (2017)

Transition metal and reductant free α-C(sp3)-H hydroxylation of carbonyl compounds are reported. This method is promoted by commercially available inexpensive KO-t-Bu and atmospheric air as an oxidant at room temperature. This unified strategy is also very facile for hydroxylation of various carbonyl compound derivatives to obtain quaternary hydroxyl compounds in excellent yield. A preliminary mechanistic investigation, supported by isotope labeling and computational studies, suggests the formation of a peroxide bond and its cleavage by in situ generated enolate.

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