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88015-70-7

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88015-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88015-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88015-70:
(7*8)+(6*8)+(5*0)+(4*1)+(3*5)+(2*7)+(1*0)=137
137 % 10 = 7
So 88015-70-7 is a valid CAS Registry Number.

88015-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butyloctanal

1.2 Other means of identification

Product number -
Other names 2-hexylhexanal

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:88015-70-7 SDS

88015-70-7Downstream Products

88015-70-7Relevant articles and documents

Recycling of two molecular catalysts in the hydroformylation/aldol condensation tandem reaction using one multiphase system

Leitner, Walter,Strohmann, Marc,Vorholt, Andreas J.,Vossen, Jeroen T.

, p. 8444 - 8451 (2021/01/01)

Tandem reactions are of great importance to efficiently execute multiple conversions in one synthesis step. Herein we present a multiphase system for the hydroformylation/aldol condensation, which is able to recycle both optimized catalysts multiple times. The system consists of an organometallic rhodium/sulfoXantphos hydroformylation catalyst and basic NaOH as aldol condensation initiator, which are both immobilized in a polyethylene glycol phase. Under reaction conditions, NaOH is converted to sodium formate, which is still able to catalyse the aldol condensation. The reaction and recycling are demonstrated by the conversion of 1-pentene to the corresponding aldol product in a recycling experiment. During nine consecutive runs, no significant loss of activity is found with an overall TON of 8700 in regard to the rhodium catalyst and an average rhodium leaching of only of 0.07% per run is observed.

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