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69078-23-5

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69078-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69078-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,7 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69078-23:
(7*6)+(6*9)+(5*0)+(4*7)+(3*8)+(2*2)+(1*3)=155
155 % 10 = 5
So 69078-23-5 is a valid CAS Registry Number.

69078-23-5SDS

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 tetraoctylazanium,fluoride

1.2 Other means of identification

Product number -
Other names TETRAOCTYLAMMONIUM FLUORIDE

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:69078-23-5 SDS

69078-23-5Downstream Products

69078-23-5Relevant articles and documents

Unraveling the cation and anion effects and kinetics for ionic liquid catalyzed direct synthesis of methyl acrylate under mild conditions

Wang, Gang,Li, Zengxi,Li, Chunshan,Zhang, Suojiang

, p. 7913 - 7923 (2020/12/01)

The direct synthesis of methyl acrylate (MA) from methyl acetate and trioxane at 350-380 °C is regarded as a supplementary route for the industrial propylene oxidation process; however, it suffers from rapid catalyst deactivation. Herein, a novel ionic liquid catalyzed mild liquid-phase system was developed for the direct synthesis of MA from methyl acetate and trioxane, where N,O-bis(trimethylsilyl)acetamide (BSA) was used as a probase for α-deprotonation and enol silyl etherification of methyl acetate. The trioxane decomposition to formaldehyde and methyl acetate enolization to 1-methoxy-1-trimethylsilyloxyethene proceeded with the catalysis of [Cation]Cl/MClx (M = Cu+, Fe3+, Zn2+ and Al3+) and [Cation]F, respectively. The cations and anions were observed to have significant effects on the yield and selectivity of MA, owing to the steric hindrance, acid site category and strength confirmed by pyridine probing FT-IR characterization. As a result, up to 60.2% yield with 94.6% selectivity of MA could be achieved when [N3,3,3,3]F and [N3,3,3,3]Cl/AlCl3 with 67 mol% AlCl3 were used in the presence of BSA at 25 °C. Kinetic studies indicated that the trioxane decomposition with the activation barrier of 41.2 ± 0.3 kJ mol-1 was the rate-determining step.

Convenient Procedures for the Preparation of Lipophilic Quaternary Onium Fluorides, Hydrogendifluorides and Dihydrogentrifluorides via Ion Exchange in Two-Phase Systems

Landini, Dario,Molinari, Henriette,Penso, Michele,Rampoldi, Alessandro

, p. 953 - 955 (2007/10/02)

A series of lipophilic quaternary onium fluorides 2, hydrogendifluorides 3, and dihydrogentrifluorides 4 are easily synthesized in almost quantitative yields from the corresponding quaternary hydrogen sulfates by exchange with the appropriate anion in an organic aqueous two-phase system; alternatively quaternary salts 4 can be prepared from onium chlorides 5 or bromides 6 under the same conditions.

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