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(2S,3R)-2-(chloromethyl)-3-{4-[(4-methoxyphenyl)methoxy]butyl}oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1278553-39-1 Structure
  • Basic information

    1. Product Name: (2S,3R)-2-(chloromethyl)-3-{4-[(4-methoxyphenyl)methoxy]butyl}oxirane
    2. Synonyms: (2S,3R)-2-(chloromethyl)-3-{4-[(4-methoxyphenyl)methoxy]butyl}oxirane
    3. CAS NO:1278553-39-1
    4. Molecular Formula:
    5. Molecular Weight: 284.783
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1278553-39-1.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: (2S,3R)-2-(chloromethyl)-3-{4-[(4-methoxyphenyl)methoxy]butyl}oxirane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3R)-2-(chloromethyl)-3-{4-[(4-methoxyphenyl)methoxy]butyl}oxirane(1278553-39-1)
    11. EPA Substance Registry System: (2S,3R)-2-(chloromethyl)-3-{4-[(4-methoxyphenyl)methoxy]butyl}oxirane(1278553-39-1)
  • 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: 1278553-39-1(Hazardous Substances Data)

1278553-39-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1278553-39-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,8,5,5 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1278553-39:
(9*1)+(8*2)+(7*7)+(6*8)+(5*5)+(4*5)+(3*3)+(2*3)+(1*9)=191
191 % 10 = 1
So 1278553-39-1 is a valid CAS Registry Number.

1278553-39-1Relevant articles and documents

An iterative acetylene-epoxide coupling strategy for the total synthesis of aspinolide A

Sabitha, Gowravaram,Reddy, Teega Rammohan,Srinivas, Chitti,Yadav, Jhillu Singh

, p. 224 - 229 (2011)

The total synthesis of aspinolide A (1) was successfully achieved by an iterative acetylene-epoxide coupling strategy and a Yamaguchi lactonization as the key steps.

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