Welcome to LookChem.com Sign In|Join Free
  • or
(R)-ethyl 4-[(tert-butoxycarbonyl)amino]-3-(4-chlorophenyl)butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

625457-56-9

Post Buying Request

625457-56-9 Suppliers

Recommended suppliers

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

625457-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 625457-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,5,4,5 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 625457-56:
(8*6)+(7*2)+(6*5)+(5*4)+(4*5)+(3*7)+(2*5)+(1*6)=169
169 % 10 = 9
So 625457-56-9 is a valid CAS Registry Number.

625457-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-ethyl 4-[(tert-butoxycarbonyl)amino]-3-(4-chlorophenyl)butanoate

1.2 Other means of identification

Product number -
Other names -

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:625457-56-9 SDS

625457-56-9Downstream Products

625457-56-9Relevant academic research and scientific papers

Enantioselective Syntheses of (-)-(R)-Rolipram, (-)-(R)-Baclofen and Other GABA Analogues via Rhodium-Catalyzed Conjugate Addition of Arylboronic Acids

Becht, Jean-Michel,Meyer, Oliver,Helmchen, Guenter

, p. 2805 - 2810 (2007/10/03)

Highly enantioselective syntheses of two important γ-aminobutyric acid (GABA) analogues, the antispastic drug (-)-(R)-Baclofen and the antidepressant agent (-)-(R)-Rolipram, are reported. Key-steps in both syntheses are the Rh-catalyzed asymmetric 1,4-additions of arylboronic acids to 4-aminobut-2,3-enoic acid derivatives.

Enantioselective synthesis of (-)-(R)-Baclofen and analogues via rhodium-catalysed conjugate addition of boronic acids

Meyer, Oliver,Becht, Jean-Michel,Helmchen, Günter

, p. 1539 - 1541 (2007/10/03)

Highly enantioselective syntheses of the antispastic drug (-)-(R)-Baclofen and analogues have been achieved by using rhodium-catalysed asymmetric 1,4-additions of arylboronic acids to 4-amino-but-2,3-enoic acid derivatives.

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 625457-56-9