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405878-89-9

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405878-89-9 Usage

Structure

Contains a pyrrolidin-2,5-dione ring with a 3,3,3-trifluoropropyl side chain attached.

Type

Ester compound

Applications

Synthesis of pharmaceuticals
Synthesis of agrochemicals
Reagent in organic synthesis

Unique Features

Unique reactivity
Stability

Functional Group

Trifluoropropyl group

Chemical Functionality

Modifies properties of other compounds

Versatility

Wide applications in chemistry and chemical engineering.

Check Digit Verification of cas no

The CAS Registry Mumber 405878-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,8,7 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 405878-89:
(8*4)+(7*0)+(6*5)+(5*8)+(4*7)+(3*8)+(2*8)+(1*9)=179
179 % 10 = 9
So 405878-89-9 is a valid CAS Registry Number.

405878-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,3-trifluoroacetic acid N-hydroxysuccinimide ester

1.2 Other means of identification

Product number -
Other names 3,3,3-trifluoropropionic acid 2,5-dioxo-pyrrolidin-1-yl 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:405878-89-9 SDS

405878-89-9Relevant articles and documents

An efficient sequence for the preparation of small secondary amine hydrochloride salts for focused library generation without need for distillation or chromatographic purification

Dubowchik, Gene M.,Michne, Jodi A.,Zuev, Dmitry

, p. 3147 - 3149 (2007/10/03)

Collections of small secondary amines for compound library generation can be efficiently prepared by amide reduction using BH3-THF or Red-Al followed by brief methanolysis, trapping with di-tert-butyl dicarbonate, and deprotection with 4M HCl i

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