Welcome to LookChem.com Sign In|Join Free

CAS

  • or

75834-11-6

Pyrrolidine, 2-(methoxymethyl)-1-[(2E)-3-phenyl-2-propenyl]-, (2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75834-11-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 75834-11-6 Structure

  • Basic information

    1. Product Name: Pyrrolidine, 2-(methoxymethyl)-1-[(2E)-3-phenyl-2-propenyl]-, (2S)-
    2. Synonyms:
    3. CAS NO:75834-11-6
    4. Molecular Formula: C15H21NO
    5. Molecular Weight: 231.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75834-11-6.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: Pyrrolidine, 2-(methoxymethyl)-1-[(2E)-3-phenyl-2-propenyl]-, (2S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrrolidine, 2-(methoxymethyl)-1-[(2E)-3-phenyl-2-propenyl]-, (2S)-(75834-11-6)
    11. EPA Substance Registry System: Pyrrolidine, 2-(methoxymethyl)-1-[(2E)-3-phenyl-2-propenyl]-, (2S)-(75834-11-6)

  • 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: 75834-11-6(Hazardous Substances Data)

75834-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75834-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,3 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75834-11:
(7*7)+(6*5)+(5*8)+(4*3)+(3*4)+(2*1)+(1*1)=146
146 % 10 = 6
So 75834-11-6 is a valid CAS Registry Number.

75834-11-6Relevant articles and documents

Chiral Homoenolate Equivalents, II. - Asymmetric Synthesis of 3-Substituted 3-Phenylpropionaldehydes via Metallated Chiral Cinnamylamines

Ahlbrecht, Hubertus,Enders, Dieter,Santowski, Ludger,Zimmermann, Gerd

, p. 1995 - 2004 (2007/10/02)

The diastereomeric excess obtained in alkylation reactions of the chiral homoenolate equivalent 22 with prolinol ether as chiral auxiliary leading to the formation of phenylpropionaldehydes 24 depends strongly on the solvent used.The structure of the alkylating reagent on the other hand is not important.The best results (about 9:1) are obtained in tert-butyl methyl ether as solvent.Other chiral auxiliaries testet were uneffective. - Key Words: Chiral homoenolate equivalents / Alkylation / Chiral 1-aminoallyl anions / Chiral aldehydes

CHIRAL HOMOENOLATE EQUIVALENTS. I. ASYMMETRIC SYNTHESIS OF β-SUBSTITUTED ALDEHIDES VIA METALATED CHIRAL ALLYLAMINES

Ahlbrecht, Hubertus,Bonnet, Gerhard,Enders, Dieter,Zimmermann, Gerd

, p. 3175 - 3178 (2007/10/02)

Metalated chiral allylamines of type 2 (M = Li, K) are used as chiral homoenolate equivalents and allow after alkylation and acidic hydrolysis asymmetric C-C bond formations to β-substituted aldehydes in enantiomeric excesses up to 67percent.

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 75834-11-6