Welcome to LookChem.com Sign In|Join Free
  • or
2-Propenoic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68185-02-4

Post Buying Request

68185-02-4 Suppliers

Recommended suppliers

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

68185-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68185-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,8 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68185-02:
(7*6)+(6*8)+(5*1)+(4*8)+(3*5)+(2*0)+(1*2)=144
144 % 10 = 4
So 68185-02-4 is a valid CAS Registry Number.

68185-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(phenylmethoxycarbonylamino)prop-2-enoate

1.2 Other means of identification

Product number -
Other names N-Carbobenzoxy-2,3-dihydroalaninaethylester

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:68185-02-4 SDS

68185-02-4Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF 2-AZABICYCLO[3.3.0]OCTANE-3-CARBOXYLIC ACID DERIVATIVES

-

Page/Page column 16, (2008/06/13)

The present invention is aimed at a process for the preparation of compounds of the general formula (I) through the hydrogeneration of cyclization of the intermediates of the formula (II)

A new and convenient method for the synthesis of dehydroamino acids starting from ethyl N-Boc- and N-Z-α-tosylglycinates and various nitro compounds

Nagano, Tanemasa,Kinoshita, Hideki

, p. 1605 - 1613 (2007/10/03)

Ethyl N-Boc- and N-Z-α-tosylglycinates, which were readily available from t-butyl or benzyl carbamate, ethyl glyoxylate, and sodium p- toluenesulfinate in formic acid, were reacted with a variety of nitro compounds in the presence of a base to afford the corresponding α,β- didehydroamino acid derivatives in good yields. Eventually, it was found that the (Z)-isomer was predominantly formed in the present method.

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 68185-02-4