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4-Cycloocten-1-carboxaldehyd is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19835-69-9

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19835-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19835-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,3 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19835-69:
(7*1)+(6*9)+(5*8)+(4*3)+(3*5)+(2*6)+(1*9)=149
149 % 10 = 9
So 19835-69-9 is a valid CAS Registry Number.

19835-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclooct-4-ene-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-Cyclooctene-1-carboxaldehyde

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:19835-69-9 SDS

19835-69-9Relevant academic research and scientific papers

Methods of providing a fragrance to a composition and methods of enhancing fragrances using cyclooctadiene hydroformylation products

-

, (2008/06/13)

The use of aldehydes as odorous materials, which can be produced through partial or total hydroformylation of cyclooctadienes, except cyclooctane aldehydes, is described. The fragrance enhancing capacity of the compounds is described in methods for their use both as perfumes and perfume enhancers or boosters.

Rhodium complex catalyzed hydroformylation reactions of linear and cyclic mono- and diolefins

Trzeciak, Anna M.,Ziolkowski, Jozef J.

, p. 213 - 216 (2007/10/02)

The hydroformylation reactions of cyclopentene, cyclohexene, 4-vinylcyclohexene, cycloheptene and cyclooctene, catalyzed with a Rh(acac)2/P(OPh)3 (I) system at 80 deg C and 10 atm (CO+H2), have been studied.Only cyclopentene and 4-vinylcyclohexene undergo hydroformylation at 1 atm and 40 deg C.The hydroformylation of some cyclic dienes; (1,3- and 1,4-cyclohexadienes, 1,3- and 1,5-cyclooctadienes and 1,3-cyclopentadiene), at 10 atm and 80 deg C, was investigated in two catalytic systems: (I) and Rh(acac) (CO) (PPh3) / PPh3 (II).The main reaction products of cyclohexadienes and pentadiene (at 80 deg C, 10 atm) are unsaturated monoaldehydes.In hydroformylation of 1,5-cyclooctadiene the main product is formylcyclooctane.Key words: Rhodium; Olefins; Hydroformylation

SELECTIVE HYDROFORMYLATION OF CYCLODIENES TO CYCLOALKENECARBOXALDEHYDES USING CATALYSTS DERIVED DIRECTLY FROM Rh VAPOUR AND CYCLODIENES

Salvadori, Piero,Vitulli, Giovanni,Raffaelli, Andrea,Lazzaroni, Raffaello

, p. 351 - 356 (2007/10/02)

Cocondensation of Rh atoms with cyclodienes at liquid nitrogen temperature yields Rh complexes, thermally stable in excess of the ligand, which are good catalysts for the selective hydroformylation of cyclodienes to cycloalkenecarboxaldehydes.

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