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1,2-Hydrazinedicarboxylic acid, 1-(phenylmethyl)-, 2-(1,1-dimethylethyl) 1-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57699-63-5

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57699-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57699-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,9 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57699-63:
(7*5)+(6*7)+(5*6)+(4*9)+(3*9)+(2*6)+(1*3)=185
185 % 10 = 5
So 57699-63-5 is a valid CAS Registry Number.

57699-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[benzyl(3,3-dimethylbutoxycarbonyl)amino]carbamate

1.2 Other means of identification

Product number -
Other names N-t-butoxycarbonyl-azaphenylalanine 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:57699-63-5 SDS

57699-63-5Relevant academic research and scientific papers

The efficient synthesis of azaamino acids

Wieczerzak,Kozlowska,Lankiewicz,Grzonka

, p. 1693 - 1697 (2007/10/03)

An efficient method of synthesis of N-t-butoxycarbonyl-azaamino acid ethyl esters has been described. This method consisted of three stages including: hydrazone formation, its reduction and acylation with ethyl chloroformate. The second step - reduction of the hydrazones to the appropriate hydrazides - was the most challenging. Some reducing agents have been tested, though NaBH3CN was found to lead to the final products with the highest yields in relatively short time and even to allow the selective reduction of C-N bond in the presence of nitro group.

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