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1260146-52-8

(R)-1-hydroxy-3-methyl-1-phenylbutan-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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  • 1260146-52-8 Structure

  • Basic information

    1. Product Name: (R)-1-hydroxy-3-methyl-1-phenylbutan-2-one
    2. Synonyms: (R)-1-hydroxy-3-methyl-1-phenylbutan-2-one
    3. CAS NO:1260146-52-8
    4. Molecular Formula:
    5. Molecular Weight: 178.231
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1260146-52-8.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: (R)-1-hydroxy-3-methyl-1-phenylbutan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-1-hydroxy-3-methyl-1-phenylbutan-2-one(1260146-52-8)
    11. EPA Substance Registry System: (R)-1-hydroxy-3-methyl-1-phenylbutan-2-one(1260146-52-8)

  • 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: 1260146-52-8(Hazardous Substances Data)

1260146-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1260146-52-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,1,4 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1260146-52:
(9*1)+(8*2)+(7*6)+(6*0)+(5*1)+(4*4)+(3*6)+(2*5)+(1*2)=118
118 % 10 = 8
So 1260146-52-8 is a valid CAS Registry Number.

1260146-52-8Downstream Products

1260146-52-8Relevant articles and documents

Benzaldehyde lyase-catalyzed diastereoselective C-C bond formation by simultaneous carboligation and kinetic resolution

Müller, Christoph R.,Pérez-Sánchez, María,Domínguez De María, Pablo

supporting information, p. 2000 - 2004 (2013/05/22)

Enzymes create chiral microenvironments that may simultaneously generate several stereogenic centers in the same catalytic cycle, broadening the possibilities of biocatalysis. Benzaldehyde lyase (BAL) affords highly diastereoselective α-hydroxy-ketones by simultaneously performing ligation and kinetic resolution of a racemic aldehyde. Thus, to the well-known enantioselective BAL-carboligation of aldehydes (C-C bond formation), another property, namely diastereoselectivity, is added in this paper for the first time.

Enantioselective aerobic oxidation of α-hydroxy-ketones catalyzed by oxidovanadium(V) methoxides bearing chiral, N-salicylidene- tert -butylglycinates

Chen, Chien-Tien,Kao, Jun-Qi,Salunke, Santosh B.,Lin, Ya-Hui

, p. 26 - 29 (2011/03/22)

Chiral oxidovanadium(V) methoxides prepared from 3,5-disubstituted-N- salicylidene-l-tert-butylglycines and vanadyl sulfate in air-saturated MeOH serve as highly enantioselective catalysts for asymmetric aerobic oxidations and kinetic resolution of alkyl, aryl, and heteroaryl α-hydroxy-ketones with differed α-substituents at ambient temperature in toluene or TBME (tert-butyl methyl ether). The best scenarios involve the use of complexes which bear the tridendate templates derived from 3,5-diphenyl- or 3-o-biphenyl-5-nitro-salicyaldehyde. The kinetic resolution selectivities of the aerobic oxidation process are in the range of 12 to >1000 based on the selectivity factors (krel).

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