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CAS

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85000-03-9

(3R)-4-Methyl-3-phenylpentyl-acetat is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85000-03-9 Structure

  • Basic information

    1. Product Name: (3R)-4-Methyl-3-phenylpentyl-acetat
    2. Synonyms:
    3. CAS NO:85000-03-9
    4. Molecular Formula:
    5. Molecular Weight: 220.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85000-03-9.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: (3R)-4-Methyl-3-phenylpentyl-acetat(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R)-4-Methyl-3-phenylpentyl-acetat(85000-03-9)
    11. EPA Substance Registry System: (3R)-4-Methyl-3-phenylpentyl-acetat(85000-03-9)

  • 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: 85000-03-9(Hazardous Substances Data)

85000-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85000-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85000-03:
(7*8)+(6*5)+(5*0)+(4*0)+(3*0)+(2*0)+(1*3)=89
89 % 10 = 9
So 85000-03-9 is a valid CAS Registry Number.

85000-03-9Downstream Products

85000-03-9Relevant articles and documents

A NEW AND EFFECTIVE ASYMMETRIC SYNTHESIS OF 3-PHENYLALKANALS

Mukaiyama, Teruaki,Hayashi, Hiroki,Miwa, Tetsuo,Narasaka, Koichi

, p. 1637 - 1640 (2007/10/02)

Highly optically active 3-phenylalkanals were obtained by the reaction of alkyl halides and a chiral homoenolate equivalent derived from the cinnamyl ether 3 and potassium diisopropylamide, followed by acidic hydrolysis.

CHIRAL HOMOENOLATE EQUIVALENTS. I. ASYMMETRIC SYNTHESIS OF β-SUBSTITUTED ALDEHIDES VIA METALATED CHIRAL ALLYLAMINES

Ahlbrecht, Hubertus,Bonnet, Gerhard,Enders, Dieter,Zimmermann, Gerd

, p. 3175 - 3178 (2007/10/02)

Metalated chiral allylamines of type 2 (M = Li, K) are used as chiral homoenolate equivalents and allow after alkylation and acidic hydrolysis asymmetric C-C bond formations to β-substituted aldehydes in enantiomeric excesses up to 67percent.

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