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1415121-99-1

(3R,6S)-6-benzyloxy-3-hydroxy-2,8-dimethyl-1-nonen-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1415121-99-1 Structure

  • Basic information

    1. Product Name: (3R,6S)-6-benzyloxy-3-hydroxy-2,8-dimethyl-1-nonen-5-one
    2. Synonyms: (3R,6S)-6-benzyloxy-3-hydroxy-2,8-dimethyl-1-nonen-5-one
    3. CAS NO:1415121-99-1
    4. Molecular Formula:
    5. Molecular Weight: 290.403
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1415121-99-1.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: (3R,6S)-6-benzyloxy-3-hydroxy-2,8-dimethyl-1-nonen-5-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,6S)-6-benzyloxy-3-hydroxy-2,8-dimethyl-1-nonen-5-one(1415121-99-1)
    11. EPA Substance Registry System: (3R,6S)-6-benzyloxy-3-hydroxy-2,8-dimethyl-1-nonen-5-one(1415121-99-1)

  • 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: 1415121-99-1(Hazardous Substances Data)

1415121-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415121-99-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,1,2 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1415121-99:
(9*1)+(8*4)+(7*1)+(6*5)+(5*1)+(4*2)+(3*1)+(2*9)+(1*9)=121
121 % 10 = 1
So 1415121-99-1 is a valid CAS Registry Number.

1415121-99-1Downstream Products

1415121-99-1Relevant articles and documents

Stereoselective titanium-mediated aldol reactions of α-benzyloxy methyl ketones

Pellicena, Miquel,Solsona, Joan G.,Romea, Pedro,Urpi, Felix

, p. 10338 - 10350,13 (2012/12/12)

Good levels of 1,4-anti asymmetric induction are obtained in the TiCl 3(i-PrO)-mediated aldol reaction of chiral α-benzyloxy methyl ketones with a wide array of aldehydes. This methodology represents a new approach to substrate-controlled acetate aldol reactions capable of providing highly functionalized fragments in a straightforward manner, which may be useful in the design of more efficient syntheses.

Stereoselective titanium-mediated aldol reactions of α-benzyloxy methyl ketones

Pellicena, Miquel,Solsona, Joan G.,Romea, Pedro,Urpí, Fèlix

, p. 10338 - 10350 (2013/01/15)

Good levels of 1,4-anti asymmetric induction are obtained in the TiCl 3(i-PrO)-mediated aldol reaction of chiral α-benzyloxy methyl ketones with a wide array of aldehydes. This methodology represents a new approach to substrate-controlled acetate aldol reactions capable of providing highly functionalized fragments in a straightforward manner, which may be useful in the design of more efficient syntheses.

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