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1H-Telluroxanthene-4-carboxaldehyde, 2,3,5,6,7,8-hexahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65342-60-1

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65342-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65342-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,4 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65342-60:
(7*6)+(6*5)+(5*3)+(4*4)+(3*2)+(2*6)+(1*0)=121
121 % 10 = 1
So 65342-60-1 is a valid CAS Registry Number.

65342-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,6,7,8-hexahydro-1H-telluroxanthene-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1H-Telluroxanthene-4-carboxaldehyde,2,3,5,6,7,8-hexahydro

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:65342-60-1 SDS

65342-60-1Downstream Products

65342-60-1Relevant academic research and scientific papers

Synthesis, structure and reactivity of β-chalcocyclohexenals: Dichalcogenides and chalcogenides

Prasad, Poonam R.,Singh, Harkesh B.,Butcher, Ray J.

, p. 42 - 56 (2016/05/19)

The present work describes the synthesis and characterization of a series of organochalcogen compounds derived from β-chlorocyclohexenal (27a)/β-bromocyclohexenal (27b) which are stabilized by E...O (E = S, Se, Te) intramolecular secondary bonding interaction (IM-SBI). Di-(2-formylcyclohex-1-ene)sulfide (21) was prepared by treating 27b with disodium sulfide. Di-(2-formylcyclohex-1-ene)diselenide (28) was obtained by reacting 27a with disodium diselenide. The reaction always produced a mixture of di-(2-formylcyclohex-1-ene)diselenide (28) and di-(2-formylcyclohex-1-ene)selenide (29). Attempts to synthesize di-(2-formylcyclohex-1-ene)ditelluride 30 by the reaction of 27b with disodium ditelluride afforded a mixture of monotellurides; 3,4,5,6,7,8-hexahydro-2H-9-telluraanthracene-1-carbaldehyde (26), di-(2-formylcyclohex-1-ene)telluride (22) and 9-hydroxy-2,3,5,6,7,8,9,9a-octahydro-1H-telluroxanthene-4-carbaldehyde (31). Reactions of 28 with halogenating reagents afforded the corresponding organylselenenyl halides; selenenyl chloride 35, selenenyl bromide 36 and selenenyl iodide 37. Tellurides 26 and 22 were used as ligands for metal complexation reactions.

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