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2-Hydroxyhexahydro-1H-isoindole-1,3(2H)-dione is a complex organic compound with the molecular formula C7H11NO3. It is a cyclic structure with a hexahydroisoindole core, which consists of a six-membered ring with one nitrogen atom and five carbon atoms. The compound features a hydroxyl group (-OH) attached to the second carbon atom and a 1,3-dione functional group, which includes two carbonyl groups (C=O) at the first and third carbon atoms. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

5426-10-8

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5426-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5426-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5426-10:
(6*5)+(5*4)+(4*2)+(3*6)+(2*1)+(1*0)=78
78 % 10 = 8
So 5426-10-8 is a valid CAS Registry Number.

5426-10-8SDS

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 N-hydroxyhexahydrophthalimide

1.2 Other means of identification

Product number -
Other names N-Hydroxy-cyclohexan-1,2-dicarbonsaeureimid

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:5426-10-8 SDS

5426-10-8Downstream Products

5426-10-8Relevant academic research and scientific papers

Monomer having electron-withdrawing group and process for preparing the same

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, (2008/06/13)

A monomer containing an electron-withdrawing group of the present invention is represented by following Formula (a), (b) or (c): wherein A1, A2, and A3 are each a ring; Ra, Rb, Rc, and Ru are the same or different and are each a hydrogen atom or organic group; at least one of Rs, Rw and Rv, at least one of Rt and Rw1, and at least one of the two Rw2s are each an electron-withdrawing group, and the others are each a hydrogen atom or organic group; W1 is a single bond or linkage group; and n denotes an integer of 2 to 25, where at least two of Ra, Rb, Rc, Rs, Rt, Ru, Rv, Rw, Rw1, Rw2, W1, and carbon atoms constituting ring A1, carbon atoms constituting ring A2, and carbon atoms constituting ring A3 may be combined to form a ring, respectively. The electron-withdrawing groups in Rs, Rt, Rv, Rw, Rw1, and Rw2 are, for example, groups each containing a fluorine atom. The monomer is useful as a raw material for photoresist polymeric compounds.

Method for the preparation of a N-alkoxy-(tetra-or hexahydro)-phthalimide and method for the preparation of a N-alkoxyamine

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, (2008/06/13)

Method for the preparation of N-alkoxy-(tetra- or hexahydro)-phthalimide according to formula I STR1 R1 being methyl or ethyl and R2 and R3 being each independently of one another hydrogen or alkyl with 1-4 C atoms or R2 and R3 together with the carbon atom to which they are bonded forming a ring with 5 or 6 C atoms, wherein the salt of the corresponding N-hydroxy-(tetrahydro- or hexahydro)-phthalimide according to formula II: STR2 with R2 and R3 as defined above and M being an alkali metal, is brought into contact with R1 Cl as alkylating agent, wherein R1 has the aforementioned meaning. The N-alkoxy-(tetra- or hexahydro)-phthalimide can afterwards be converted with the aid of hydroxylamine sulphate into the corresponding alkoxyamine after which the alkoxyamine obtained can be isolated. In this manner a simple and commercially attractive process for the preparation of O-(m)ethylhydroxylamine can be implemented.

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