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1196871-20-1

methyl (2S)-2-(benzyloxy)-2-[(R)-hydroxy(phenyl)methyl]butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1196871-20-1 Structure

  • Basic information

    1. Product Name: methyl (2S)-2-(benzyloxy)-2-[(R)-hydroxy(phenyl)methyl]butanoate
    2. Synonyms:
    3. CAS NO:1196871-20-1
    4. Molecular Formula:
    5. Molecular Weight: 314.381
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1196871-20-1.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: methyl (2S)-2-(benzyloxy)-2-[(R)-hydroxy(phenyl)methyl]butanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2S)-2-(benzyloxy)-2-[(R)-hydroxy(phenyl)methyl]butanoate(1196871-20-1)
    11. EPA Substance Registry System: methyl (2S)-2-(benzyloxy)-2-[(R)-hydroxy(phenyl)methyl]butanoate(1196871-20-1)

  • 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: 1196871-20-1(Hazardous Substances Data)

1196871-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1196871-20-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,8,7 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1196871-20:
(9*1)+(8*1)+(7*9)+(6*6)+(5*8)+(4*7)+(3*1)+(2*2)+(1*0)=191
191 % 10 = 1
So 1196871-20-1 is a valid CAS Registry Number.

1196871-20-1Upstream product

1196871-20-1Downstream Products

1196871-20-1Relevant articles and documents

Enantioselective aldol reaction of tetrasubstituted ketene silyl acetals with achiral aldehydes for the construction of asymmetric tertiary alcohols: An application for the divergent total syntheses of buergerinins F and G

Shiina, Isamu,Iizumi, Takashi,Yamai, Yu-Suke,Kawakita, Yo-Ichi,Yokoyama, Kazutoshi,Yamada, Yo-Ko

, p. 2915 - 2926 (2009)

The asymmetric aldol reaction of heteroatom-substituted ketene silyl acetals with achiral aldehydes has been developed by the promotion of tin(II) triflate coordinated with a chiral diamine to afford the corresponding aldols having chiral tertiary alcohol

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