Welcome to LookChem.com Sign In|Join Free
  • or
1-Pyrrolidinecarboxylic acid, 2-ethoxy-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106412-39-9

Post Buying Request

106412-39-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

106412-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106412-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,1 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106412-39:
(8*1)+(7*0)+(6*6)+(5*4)+(4*1)+(3*2)+(2*3)+(1*9)=89
89 % 10 = 9
So 106412-39-9 is a valid CAS Registry Number.

106412-39-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 2-ethoxypyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-benzyloxycarbonyl-2-ethoxypyrrolidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:106412-39-9 SDS

106412-39-9Relevant academic research and scientific papers

Design, synthesis and SAR studies of GABA uptake inhibitors derived from 2-substituted pyrrolidine-2-yl-acetic acids

Steffan, Tobias,Renukappa-Gutke, Thejavathi,H?fner, Georg,Wanner, Klaus T.

, p. 1284 - 1306 (2015)

In this paper, we disclose the design and synthesis of a series of 2-substituted pyrrolidine-2-yl-acetic acid as core structures and the N-arylalkyl derivatives thereof as potential GABA transport inhibitors. The 2-position in the side chain of pyrrolidin

Catalytic Asymmetric Additions of Enol Silanes to In Situ Generated Cyclic, Aliphatic N-Acyliminium Ions

Aukland, Miles H.,Grossmann, Oleg,Lee, Sunggi,List, Benjamin,Maji, Rajat

supporting information, (2022/01/19)

Strong and confined imidodiphosphorimidate (IDPi) catalysts enable highly enantioselective substitutions of cyclic, aliphatic hemiaminal ethers with enol silanes. 2-Substituted pyrrolidines, piperidines, and azepanes are obtained with high enantioselectiv

A convenient allylsilane-N-acyliminium route toward 5-alkylindolizidines. Diastereoselective synthesis of (±)-indolizidine 167B

Peroche, Sandrine,Remuson, Roland,Gelas-Mialhe, Yvonne,Gramain, Jean-Claude

, p. 4617 - 4619 (2007/10/03)

A highly diastereoselective synthesis of 5-alkylindolizidines is described via an intermolecular addition of the allylsilyl functional group of homoallylic alcohols with an N-acyliminium ion derived from pyrrolidin-2-one.

REDUCTION OF N-ALKOXYCARBONYLLACTAMS WITH NaBH4/EtOH-H+: A FACILE SYNTHESIS OF α-ETHOXYURETHANES

Nagasaka, Tatsuo,Tamano, Hirohisa,Hamaguchi, Fumiko

, p. 1231 - 1232 (2007/10/02)

Reduction of N-alkoxycarbonyllactams with NaBH4/H+ in ethanol (Speckamp's condition) afforded α-ethoxyurethanes (Shono's compounds) in good yields.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 106412-39-9