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1,3-Dioxoisoindoline-2-butyric acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10294-97-0

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10294-97-0 Usage

Type of compound

Ester

Parent acid

1,3-Dioxoisoindoline-2-butyric acid

Application

Pharmaceutical industry (building block for synthesis of bioactive compounds and drugs)

Potential properties

Anti-inflammatory and neuroprotective

Synthesis method

Organic chemical reactions

Safety handling

Standard laboratory safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 10294-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,9 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10294-97:
(7*1)+(6*0)+(5*2)+(4*9)+(3*4)+(2*9)+(1*7)=90
90 % 10 = 0
So 10294-97-0 is a valid CAS Registry Number.

10294-97-0SDS

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 ethyl 4-(1,3-dioxoisoindol-2-yl)butanoate

1.2 Other means of identification

Product number -
Other names ethyl 4-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)butanoate

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:10294-97-0 SDS

10294-97-0Downstream Products

10294-97-0Relevant academic research and scientific papers

EVALUATION OF THE N-PHTHALOYL MOIETY AS PROTECTING GROUP IN AMINOACYLPHOSPHONIC DERIVATIVES

Breuer, Eli,Safadi, Muhammad,Chorev, Michael,Gibson, Dan

, p. 239 - 246 (2007/10/02)

Reaction of dimethyl benzoylphosphonate with hydrazine hydrate gave exclusively benzhydrazide.Reaction of methyl lithium benzoylphosphonate with hydrazine hydrate gave the corresponding hydrazone (3) as a 65:35 mixture of E and Z isomers.Reaction of hydrazine hydrate with diisopropyl 4-phthalimidobutanoylphosphonate gave mainly products resulting from nucleopholic attack of hydrazine on the carbonyl of the acylphosphonate and only a small percentage of phthalhydrazide.From our results it appears that the N-phthaloyl protecting group is not suitable for the transient protection of amino groups during attempts to synthesize aminoacylphosphonates.

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