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87265-65-4

3,4-syn-3-hydroxy-5-trityloxy-2-pentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87265-65-4 Structure

  • Basic information

    1. Product Name: 3,4-syn-3-hydroxy-5-trityloxy-2-pentanone
    2. Synonyms:
    3. CAS NO:87265-65-4
    4. Molecular Formula:
    5. Molecular Weight: 374.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87265-65-4.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: 3,4-syn-3-hydroxy-5-trityloxy-2-pentanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-syn-3-hydroxy-5-trityloxy-2-pentanone(87265-65-4)
    11. EPA Substance Registry System: 3,4-syn-3-hydroxy-5-trityloxy-2-pentanone(87265-65-4)

  • 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: 87265-65-4(Hazardous Substances Data)

87265-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87265-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,6 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87265-65:
(7*8)+(6*7)+(5*2)+(4*6)+(3*5)+(2*6)+(1*5)=164
164 % 10 = 4
So 87265-65-4 is a valid CAS Registry Number.

87265-65-4Relevant articles and documents

STEREOSELECTIVE ACYCLIC KETONE REDUCTION. SYNTHESIS OF THE SYNTHONS HAVING THREE CONSECUTIVE CHIRAL CENTERS

Nakata, Tadashi,Fukui, Mineo,Ohtsuka, Hisatoshi,Oishi, Takeshi

, p. 2225 - 2232 (1984)

Four possible diastereomers of a functionalized 1,3-dimethyl-2-hydroxy unit were synthesized based on the stereoselective reduction of various acyclic ketones (i.e. reduction of β-keto ester, β-hydroxy ketone, α-hydroxy ketone, and α-silyloxy ketone) and

STEREOSELECTIVE SYNTHESIS OF THE SYNTHONS HAVING THREE CONSECTIVE CHIRAL CENTERS

Nakata, Tadashi,Fukui, Mineo,Ohtsuka, Hisatoshi,Oishi, Takeshi

, p. 2661 - 2664 (2007/10/02)

Four possible diastereomers having three consective chiral centers, R-CHMe-CHOH-CHMe-R', have been synthesized stereoselectively based on the stereoselective reduction of acyclic ketones.

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