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dihydro-5,5-dimethyl-2,2-diphenylfuran-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1201785-50-3 Structure
  • Basic information

    1. Product Name: dihydro-5,5-dimethyl-2,2-diphenylfuran-3(2H)-one
    2. Synonyms: dihydro-5,5-dimethyl-2,2-diphenylfuran-3(2H)-one
    3. CAS NO:1201785-50-3
    4. Molecular Formula:
    5. Molecular Weight: 266.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1201785-50-3.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: dihydro-5,5-dimethyl-2,2-diphenylfuran-3(2H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: dihydro-5,5-dimethyl-2,2-diphenylfuran-3(2H)-one(1201785-50-3)
    11. EPA Substance Registry System: dihydro-5,5-dimethyl-2,2-diphenylfuran-3(2H)-one(1201785-50-3)
  • 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: 1201785-50-3(Hazardous Substances Data)

1201785-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201785-50-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,7,8 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1201785-50:
(9*1)+(8*2)+(7*0)+(6*1)+(5*7)+(4*8)+(3*5)+(2*5)+(1*0)=123
123 % 10 = 3
So 1201785-50-3 is a valid CAS Registry Number.

1201785-50-3Downstream Products

1201785-50-3Relevant articles and documents

Thermolysis of 4-diazotetrahydrofuran-3-ones: Total change of reaction course compared to photolysis

Rodina, Ludmila L.,Medvedev, Jury J.,Galkina, Olesia S.,Nikolaev, Valerij A.

supporting information, p. 2993 - 3000 (2014/05/20)

Thermolysis of 2,2,5,5-tetrasubstituted 4-diazodihydrofuran-3-ones in protic (BnOH) and aprotic (DMSO) media, in contrast to photolysis, gives rise to the formation of 2,2,4,5-substituted 3(2H)-furanones as a result of 1,2-alkyl (aryl) shift. The thermal

Surprising secondary photochemical reactions observed on conventional photolysis of diazotetrahydrofuranones

Nikolaev, Valerij A.,Galkina, Olesja S.,Sieler, Jochim,Rodina, Ludmila L.

experimental part, p. 2713 - 2716 (2010/06/19)

The formation of C-H insertion products of the terminal N-atom of a diazo group into the α-S{cyrillic}N{cyrillic}-bond of tetrahydrofuran during direct photolysis of regioisomeric 2,2-dimethyl-5,5-diphenyl and 5,5-dimethyl-2,2-diphenyl-substituted 3-diazotetrahydrofuran-4-ones in THF is dictated by photochemical cycloelimination of the originally formed (1,1-dimethyl-2-oxa-3,3-diphenyl-propano)ketene and oxetanecarboxylic acid derivatives to yield benzophenone. The latter, under subsequent UV irradiation of the reaction mixture, initiates sensitized photolysis of the starting diazoketones resulting in the appearance of the insertion products with the solvent.

Photochemical reactions of regioisomeric 2,2-dimethyl-5,5-diphenyl- and 5,5-dimethyl-2,2-diphenyl-substituted diazo ketones of a tetrahydrofuran series

Rodina, Ludmila L.,Malashikhin, Sergey A.,Galkina, Olesya S.,Nikolaev, Valerij A.

experimental part, p. 1990 - 1998 (2010/01/11)

The principal direction of conventional photolysis of the regioisomeric 2,2-dimethyl-5,5-diphenyl-and 5,5-dimethyl-2,2-diphenyl-substituted 4-diazodihydrofuran-3(2H)-ones 1a and 1b, respectively, is the Wolff rearrangement, while other photochemical proce

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