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Hexahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione is a complex organic compound with the molecular formula C9H11NO3. It is a cyclic structure that features a six-membered ring with a hydroxy group attached to the nitrogen atom, forming an epoxy group. hexahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione is characterized by its unique chemical properties, which include the presence of a carbonyl group at positions 1 and 3, and an epoxy bridge between positions 4 and 7. It is synthesized through various chemical reactions and is used in the pharmaceutical and chemical industries for the production of intermediates and other specialty chemicals. Due to its specific structure, it may have potential applications in the development of new drugs or as a building block in the synthesis of more complex molecules.

6253-24-3

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6253-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6253-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6253-24:
(6*6)+(5*2)+(4*5)+(3*3)+(2*2)+(1*4)=83
83 % 10 = 3
So 6253-24-3 is a valid CAS Registry Number.

6253-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3a,4,5,6,7,7a-hexahydro-octahydro-1H-4,7-epoxyisoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names hexahydro-4,7-epioxido-isoindole-1,3-dione

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:6253-24-3 SDS

6253-24-3Upstream product

6253-24-3Downstream Products

6253-24-3Relevant academic research and scientific papers

OLEFIN CYCLISATIONS OF HINDERED α-ACYLIMINIUM IONS

Wijnberg, B. P.,Speckamp, W. N.,Oostveen, A. R. C.

, p. 209 - 217 (1982)

Stereocontrolled NaBH4/H+-reduction of 3,4-cis-disubstituted N-alkenyl imides 1-5 leads to secondary hydroxylactams.Tertiary hydroxylactams are formed via addition of MeMgCl to imides 2 and 4.HCOOH-Cyclisation of the hydroxylactams affords polycyclic piperidines through stereoselective α-acyliminium ring closure.Concomitant synchronous and stepwise cyclisation pathways are operative in the anti-periplanar addition of tertiary α-acyliminium ions to Me substituted olefins 8c and 11c.

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