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

84310-95-2

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84310-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84310-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,1 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84310-95:
(7*8)+(6*4)+(5*3)+(4*1)+(3*0)+(2*9)+(1*5)=122
122 % 10 = 2
So 84310-95-2 is a valid CAS Registry Number.

84310-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-2-(phenylmethoxycarbonylamino)butanoic acid

1.2 Other means of identification

Product number -
Other names 2-ethyl-2-benzyloxycarbonylamino-butyric acid

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:84310-95-2 SDS

84310-95-2Relevant academic research and scientific papers

GLUCOPYRANOSYL DERIVATIVE AND USE THEREOF

-

Paragraph 00227; 00310, (2019/08/12)

Provided are a glucopyranosyl derivative as a sodium-dependent glucose transporters inhibitor, especially as a SGLT1 inhibitor, a pharmaceutically acceptable salt or a stereoisomer thereof, a pharmaceutical composition thereof, and the uses of the compound and pharmaceutical composition thereof in the preparation of drugs for the treatment of diabetes and diabetes-related diseases.

Zinc promoted rapid and efficient synthesis of Fmoc- and Z-α,α-dialkylamino acids under neutral conditions

Babu, Vommina V. Suresh,Ananda, Kuppanna

, p. 70 - 74 (2007/10/03)

The introduction of Nα-9-fluorenylmethyloxycarbonyl (Fmoc) and benzyloxycarbonyl (Z) groups into α,α-dialkylamino acids is described at neutral pH using Fmoc-Cl or Z-Cl as an acylating agent respectively in the presence of activated zing powder. The reaction is simple, fast and clean. It also permits the scale up with high yields. It is completely free from protected oligomer formation, which is a known side-reaction when Schotten-Baumann procedure is followed. All the Fmoc- and Z-amino acids prepared have been fully characterized.

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