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124062-35-7

erythro-1-methoxy-2,4,4-trimethyl-1-phenylpentan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124062-35-7 Structure

  • Basic information

    1. Product Name: erythro-1-methoxy-2,4,4-trimethyl-1-phenylpentan-3-one
    2. Synonyms:
    3. CAS NO:124062-35-7
    4. Molecular Formula:
    5. Molecular Weight: 234.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124062-35-7.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: erythro-1-methoxy-2,4,4-trimethyl-1-phenylpentan-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: erythro-1-methoxy-2,4,4-trimethyl-1-phenylpentan-3-one(124062-35-7)
    11. EPA Substance Registry System: erythro-1-methoxy-2,4,4-trimethyl-1-phenylpentan-3-one(124062-35-7)

  • 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: 124062-35-7(Hazardous Substances Data)

124062-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124062-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,6 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124062-35:
(8*1)+(7*2)+(6*4)+(5*0)+(4*6)+(3*2)+(2*3)+(1*5)=87
87 % 10 = 7
So 124062-35-7 is a valid CAS Registry Number.

124062-35-7Downstream Products

124062-35-7Relevant articles and documents

DIASTEREOSELECTIVE ALDOL SYNTHESIS USING ACETAL TEMPLATES

Ishihara, Kazuaki,Yamamoto, Hisashi,Heathcock, Clayton H.

, p. 1825 - 1828 (2007/10/02)

Stereoselectivity of the Mukaiyama reaction is dramatically changed by the steric features of acetal structures.

TRIMETHYLSILYL TRIFLATE CATALYZED ALDOL-TYPE REACTION OF ENOL SILYL ETHERS AND ACETALS OR RELATED COMPOUNDS

Murata, Shizuaki,Suzuki, Chikusa,Noyori, Ryoji

, p. 4259 - 4276 (2007/10/02)

Trimethylsilyl triflate with or without added hindered tertiary amines catalyzes directed condensation of enol trimethylsilyl ethers with acetals, orthoformate, or 2-acetoxytetrahydrofuran or -pyrans to give the corresponding β-alkoxy carbonyl compounds.R

TRIMETHYLSILYL TRIFLATE IN ORGANIC SYNTHESIS

Noyori, R.,Murata, S.,Suzuki, M.

, p. 3899 - 3910 (2007/10/02)

Trimethylsilyl triflate is a powerful silylating agent for organic compounds and acts as a catalyst which accelerates a variety of nucleophilic reactions in aprotic media.The reactions proceed via one-center, electrophilic coordination of the silyl group to hetero functional groups and exhibit unique selectivities.

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