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74927-23-4

(2S,3S)-1-Benzyloxymethoxy-2-methyl-heptan-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74927-23-4 Structure

  • Basic information

    1. Product Name: (2S,3S)-1-Benzyloxymethoxy-2-methyl-heptan-3-ol
    2. Synonyms:
    3. CAS NO:74927-23-4
    4. Molecular Formula:
    5. Molecular Weight: 266.381
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74927-23-4.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: (2S,3S)-1-Benzyloxymethoxy-2-methyl-heptan-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3S)-1-Benzyloxymethoxy-2-methyl-heptan-3-ol(74927-23-4)
    11. EPA Substance Registry System: (2S,3S)-1-Benzyloxymethoxy-2-methyl-heptan-3-ol(74927-23-4)

  • 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: 74927-23-4(Hazardous Substances Data)

74927-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74927-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,2 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74927-23:
(7*7)+(6*4)+(5*9)+(4*2)+(3*7)+(2*2)+(1*3)=154
154 % 10 = 4
So 74927-23-4 is a valid CAS Registry Number.

74927-23-4Downstream Products

74927-23-4Relevant articles and documents

CHELATION-CONTROLLED NUCLEOPHILIC ADDITIONS. 2. A HIGHLY EFFECTIVE SYSTEM FOR ASYMMETRIC INDUCTION IN THE REACTION ON ORGANOMETALLIC WITH β-ALKOXYALDEHYDES.

Still, W. Clark,Schneider, Josef A.

, p. 1035 - 1038 (1980)

Organocuprates have been found to be highly stereoselective reagents for the addition of carbanionic nucleophiles to α-asymmetric aldehydes bearing β-oxigen substituents.The major products are those predicted by a chelation-controlled transition state and have diastereomeric purities ranging from 15-30:1.

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