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3183-23-1

3183-23-1

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3183-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3183-23-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3183-23:
(6*3)+(5*1)+(4*8)+(3*3)+(2*2)+(1*3)=71
71 % 10 = 1
So 3183-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO2.ClH/c1-4-10-7(9)5-8-6(2)3;/h6,8H,4-5H2,1-3H3;1H

3183-23-1SDS

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-(propan-2-ylamino)acetate,hydrochloride

1.2 Other means of identification

Product number -
Other names n-isopropylamino-acetic acid ethyl ester hcl

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:3183-23-1 SDS

3183-23-1Downstream Products

3183-23-1Relevant articles and documents

Base-promoted c→n acyl rearrangement: An unconventional approach to α-amino acid derivatives

Ugarriza, Iratxe,Uria, Uxue,Carrillo, Luisa,Vicario, Jose L.,Reyes, Efraim

supporting information, p. 11650 - 11654 (2014/10/15)

We have discovered that N-alkyl aminomalonates undergo a fast and selective intramolecular C→N acyl rearrangement reaction in the presence of a strong base, leading to N-protected glycinates in excellent yield. Moreover, the fact that the reaction proceeds through a nucleophilic enolate intermediate has been used for implementing a tandem rearrangement/alkylation sequence that has been applied to the preparation of synthetically relevant nonproteinogenic tertiary and quaternary N-alkyl α-amino acids in a very simple and reliable way.

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