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23659-70-3

2,3-Dihydro-2,3-dimethyl-3-phenyl-1H-isoindol-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 23659-70-3 Structure

  • Basic information

    1. Product Name: 2,3-Dihydro-2,3-dimethyl-3-phenyl-1H-isoindol-1-one
    2. Synonyms: 2,3-Dihydro-2,3-dimethyl-3-phenyl-1H-isoindol-1-one
    3. CAS NO:23659-70-3
    4. Molecular Formula:
    5. Molecular Weight: 237.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23659-70-3.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: 2,3-Dihydro-2,3-dimethyl-3-phenyl-1H-isoindol-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-Dihydro-2,3-dimethyl-3-phenyl-1H-isoindol-1-one(23659-70-3)
    11. EPA Substance Registry System: 2,3-Dihydro-2,3-dimethyl-3-phenyl-1H-isoindol-1-one(23659-70-3)

  • 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: 23659-70-3(Hazardous Substances Data)

23659-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23659-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,5 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23659-70:
(7*2)+(6*3)+(5*6)+(4*5)+(3*9)+(2*7)+(1*0)=123
123 % 10 = 3
So 23659-70-3 is a valid CAS Registry Number.

23659-70-3Downstream Products

23659-70-3Relevant articles and documents

Palladium(II)-Catalyzed C(sp2)-H Carbonylation of Sterically Hindered Amines with Carbon Monoxide

Cheng, Xiu-Fen,Wang, Tao,Li, Yan,Wu, Yun,Sheng, Jie,Wang, Rui,Li, Chao,Bian, Kang-Jie,Wang, Xi-Sheng

, p. 6530 - 6533 (2018/10/20)

A palladium-catalyzed, amine-directed C(sp2)-H carbonylation of α,α-disubstituted benzylamine under 1 atm of CO for the facile synthesis of sterically hindered benzolactam has been developed. The key to success is the use of 2,2,6,6-tetramethyl-1-piperidinyloxy as the crucial sole oxidant. The synthetic utility of this transformation has been demonstrated by the first concise synthesis of the natural product spiropachysin-20-one.

KOtBu-mediated synthesis of dimethylisoindolin-1-ones and dimethyl-5-phenylisoindolin-1-ones: Selective C-C coupling of an unreactive tertiary sp3 C-H bond

Kumar, Sangit,Bhakuni, Bhagat Singh,Yadav, Abhimanyu,Kumar, Shailesh,Patel, Saket,Sharma, Shubham

, p. 2944 - 2954 (2014/05/06)

A new reaction for the synthesis of dimethylisoindolinones has been presented from 2-halo-N-isopropyl-N-alkylbenzamide substrates and KO tBu by the selective C-C coupling of an unreactive tertiary sp 3 C-H bond. The reaction manifest

Regiochemistry in aryl radical cyclisations (5-exo versus 6-endo) of N-vinylic 2-iodobenzamides

Ishibashi, Hiroyuki,Ohata, Kohei,Niihara, Michiyo,Sato, Tatsunori,Ikeda, Masazumi

, p. 547 - 554 (2007/10/03)

Bu3SnH-mediated aryl radical cyclisations of a range of N-vinylic 2-iodobenzamides 10 were examined. The enamides 10a-d gave exclusively the 5-exo cyclisation products 11a-d, whereas the enamides 10e,f having a phenyl substituent on the vinylic carbon ato

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