Welcome to LookChem.com Sign In|Join Free

CAS

  • or

17153-02-5

rac-4-acetyl-4-methyl-2-phenyloxazol-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17153-02-5 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 17153-02-5 Structure

  • Basic information

    1. Product Name: rac-4-acetyl-4-methyl-2-phenyloxazol-5-one
    2. Synonyms: rac-4-acetyl-4-methyl-2-phenyloxazol-5-one
    3. CAS NO:17153-02-5
    4. Molecular Formula:
    5. Molecular Weight: 217.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17153-02-5.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: rac-4-acetyl-4-methyl-2-phenyloxazol-5-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: rac-4-acetyl-4-methyl-2-phenyloxazol-5-one(17153-02-5)
    11. EPA Substance Registry System: rac-4-acetyl-4-methyl-2-phenyloxazol-5-one(17153-02-5)

  • 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: 17153-02-5(Hazardous Substances Data)

17153-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17153-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,5 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17153-02:
(7*1)+(6*7)+(5*1)+(4*5)+(3*3)+(2*0)+(1*2)=85
85 % 10 = 5
So 17153-02-5 is a valid CAS Registry Number.

17153-02-5Relevant articles and documents

Asymmetric synthesis of all stereoisomers of a-methylthreonine using an organocatalytic steglich rearrangement reaction as a key step

Dietz, Friedrich R.,Groeger, Harald

, p. 4208 - 4218 (2011/04/12)

An efficient synthetic route to all four stereoisomers of a-methylthreonine has been established. Each type of stereoisomer has been isolated in diastereomerically pure form and with an enantiomeric excess of at least 86% ee. The key step in this multi-st

Novel catalytic synthetic route to protected α-methyl threonine and the first asymmetric acetyl migration in a steglich rearrangement reaction

Dietz, Friedrich R.,Gr?ger, Harald

, p. 663 - 666 (2008/12/20)

A short synthetic route to protected α-methyl threonine 5 as a representative example for (protected) α-methylated α-amino-β- hydroxy acids bearing a stereogenic quaternary carbon center in α-position was developed. This multistep synthesis is based on th

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 17153-02-5