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85000-04-0

Acetic acid (S)-3-phenyl-hex-5-enyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85000-04-0 Structure

  • Basic information

    1. Product Name: Acetic acid (S)-3-phenyl-hex-5-enyl ester
    2. Synonyms: Acetic acid (S)-3-phenyl-hex-5-enyl ester
    3. CAS NO:85000-04-0
    4. Molecular Formula:
    5. Molecular Weight: 218.296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85000-04-0.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: Acetic acid (S)-3-phenyl-hex-5-enyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid (S)-3-phenyl-hex-5-enyl ester(85000-04-0)
    11. EPA Substance Registry System: Acetic acid (S)-3-phenyl-hex-5-enyl ester(85000-04-0)

  • 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: 85000-04-0(Hazardous Substances Data)

85000-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85000-04-0 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 85000-04:
(7*8)+(6*5)+(5*0)+(4*0)+(3*0)+(2*0)+(1*4)=90
90 % 10 = 0
So 85000-04-0 is a valid CAS Registry Number.

85000-04-0Relevant articles and documents

Design, synthesis, and biological evaluation of monopyrrolinone-based HIV-1 protease inhibitors

Smith III, Amos B.,Cantin, Louis-David,Pasternak, Alexander,Guise-Zawacki, Lisa,Yao, Wenquin,Charnley, Adam K.,Barbosa, Joseph,Sprengeler, Paul A.,Hirschmann, Ralph,Munshi, Sanjeev,Olsen, David B.,Schleif, William A.,Kuo, Lawrence C.

, p. 1831 - 1844 (2007/10/03)

The design, synthesis, and biological evaluation of a series of HIV-1 protease inhibitors [(-)-6, (-)-7, (-)-23, (+)-24] based upon the 3,5,5-trisubstituted pyrrolin-4-one scaffold is described. Use of a monopyrrolinone scaffold leads to inhibitors with i

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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