Welcome to LookChem.com Sign In|Join Free

CAS

  • or

100929-22-4

(1'S,3S)-3-Hydroxy-3-phenyl-N-(1-phenylethyl)propionamid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100929-22-4 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 100929-22-4 Structure

  • Basic information

    1. Product Name: (1'S,3S)-3-Hydroxy-3-phenyl-N-(1-phenylethyl)propionamid
    2. Synonyms:
    3. CAS NO:100929-22-4
    4. Molecular Formula:
    5. Molecular Weight: 269.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100929-22-4.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: (1'S,3S)-3-Hydroxy-3-phenyl-N-(1-phenylethyl)propionamid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1'S,3S)-3-Hydroxy-3-phenyl-N-(1-phenylethyl)propionamid(100929-22-4)
    11. EPA Substance Registry System: (1'S,3S)-3-Hydroxy-3-phenyl-N-(1-phenylethyl)propionamid(100929-22-4)

  • 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: 100929-22-4(Hazardous Substances Data)

100929-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100929-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,2 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100929-22:
(8*1)+(7*0)+(6*0)+(5*9)+(4*2)+(3*9)+(2*2)+(1*2)=94
94 % 10 = 4
So 100929-22-4 is a valid CAS Registry Number.

100929-22-4Downstream Products

100929-22-4Relevant articles and documents

Stereoselective Aldol Reaction with Chiral Secondary Acetamides

Devant, Ralf,Braun, Manfred

, p. 2191 - 2207 (2007/10/02)

The deprotonated acetamides 4a - c and 5a - c are added to prochiral carbonyl compounds.The influence of the solvent, of the reaction temperature, and of the enolate gegenion on the ratio of the isomeric products 8/9, 18/19, and 26/27, respectively, are studied.The highest degree of diastereoselectivity are observed, when the titanium enolate of the acetamide 4a or the threefold deprotonated N-acetyl-α-phenylglycinol (5a) is used.The diastereomers 18a - d, formed in excess in the addition of 5a to aldehydes, are isolated in pure from by a single recrystallization, and afford the enantiomerically pure β-hydroxy carboxylic acids 3a - d.Thereby, the chiral auxiliary, α-phenylglycinol (14), is recovered.

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 100929-22-4