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116445-61-5

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116445-61-5 Usage

General Description

1-(3-chloropropyl)pyrrolidine-2,5-dione, also known as SALTDATA: FREE, is a chemical compound with the molecular formula C7H10ClNO2. It is a synthetic organic compound with potential applications in pharmaceuticals and material science. 1-(3-chloropropyl)pyrrolidine-2,5-dione(SALTDATA: FREE) contains a chlorine atom, a pyrrolidine ring, and a carbonyl group, which gives it unique properties and potential reactivity. It is important to handle this chemical with care, as it may have harmful effects if not properly managed. SALTDATA: FREE may be used in research and development of new drugs, materials, and other applications where its unique structure and properties can be advantageous.

Check Digit Verification of cas no

The CAS Registry Mumber 116445-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,4 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 116445-61:
(8*1)+(7*1)+(6*6)+(5*4)+(4*4)+(3*5)+(2*6)+(1*1)=115
115 % 10 = 5
So 116445-61-5 is a valid CAS Registry Number.

116445-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-Chloropropyl)pyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names N-(3-chloropropyl)succinimide

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:116445-61-5 SDS

116445-61-5Downstream Products

116445-61-5Relevant articles and documents

Synthesis of succinimidoalkylbenzaldehyde analogues: Potential bifunctional linkers for bioconjugation

Crosby, Ian T.,Pietersz, Geoffrey A.,Ripper, Justin A.

, p. 138 - 143 (2008)

A series of novel 4-substituted benzaldehydes containing a succinimide moiety were synthesized as potential bifunctional linkers for the purpose of binding therapeutic drugs to antibodies raised against cancer cells. These potential benzaldehyde linkers varied in the nature of the para functionality so as to provide a range of potential acid labilities. Synthesis of the linkers involved a Williamson ether formation to make the ether linker 1, a Sonagoshira palladium-catalyzed coupling to synthesize the skeleton of the alkyl linker 2, and formation of an amide bond directly from a methyl ester gave the 4-substituted amide linker 3. As an example of the type of acetal that can be produced using these linkers, uridine was used as an analogue of the cytotoxic compound 5-fluorouridine to give the cyclic acetals 19?21. CSIRO 2008.

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