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4-Cyclohexene-1,2-dicarbonyl dichloride (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52890-05-8

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52890-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52890-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,9 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52890-05:
(7*5)+(6*2)+(5*8)+(4*9)+(3*0)+(2*0)+(1*5)=128
128 % 10 = 8
So 52890-05-8 is a valid CAS Registry Number.

52890-05-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohex-4-ene-1,2-dicarbonyl chloride

1.2 Other means of identification

Product number -
Other names 4-CYCLOHEXENE-1,2-DICARBONYL DICHLORIDE

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:52890-05-8 SDS

52890-05-8Relevant academic research and scientific papers

Intramolecular Cooperative Reactions of 1,2-Bis(diazoketone)s. The First Syntheses of trans-Hydro-1H-2-inden-1-ones

Nakatani, Kazuhiko,Takada, Kazunori,Isoe, Sachihiko

, p. 2466 - 2473 (2007/10/02)

The intramolecular cooperative reactions of 1,2-bis(diazoketone)s initiated by the Wolff rearrangement of α-diazoketones have been investigated.Under thermal conditions, 1,2-bis(diazoketone)s are efficiently transformed into 2-cyclopenten-1-one derivatives with complete stereospecificity.Thus, a most extraordinary result is reported, that trans-hydro-2-inden-1-ones (1-3) were synthesized for the first time from trans-1,2-bis(diazoketone)s (5, 11, and 12), respectively.The unprecedented trans-hydroindenone structure was confirmed by X-ray analysis of 3 as well as 1H NMR analysis and was supported by ab initio molecular orbital calculations.The same reactions were also carried out under photochemical conditions and were applied to 1,3-bis(diazoketone)s, giving 2-cyclohexen-1-one derivatives.

Stereocontrolled Syntheses for the Six Diastereomeric 1,2-Dihydroxy-4,5-diaminocyclohexanes: PtII Complexes and P-388 Antitumor Properties

Witiak, Donald T.,Rotella, David P.,Filppi, Joyce A.,Gallucci, Judith

, p. 1327 - 1336 (2007/10/02)

Stereocontrolled syntheses for the six diastereomeric 1,2-dihydroxy-4,5-diaminocyclohexanes 3a-f from cyclohexene diamines cis-4 and trans-5 are described.Cbz-protected species cis-9 and trans-11, respectively, served as a source of stable Cbz-protected p

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