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2-Pentenoic acid, 4-methyl-2-[[(phenylmethoxy)carbonyl]amino]-, ethyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50685-07-9

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50685-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50685-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,8 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50685-07:
(7*5)+(6*0)+(5*6)+(4*8)+(3*5)+(2*0)+(1*7)=119
119 % 10 = 9
So 50685-07-9 is a valid CAS Registry Number.

50685-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (Z)-α-N-benzyloxycarbonyl-α,β-didehydroleucinate

1.2 Other means of identification

Product number -
Other names (Z)-2-Benzyloxycarbonylamino-4-methyl-pent-2-enoic acid ethyl ester

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:50685-07-9 SDS

50685-07-9Relevant academic research and scientific papers

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.

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