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tert-butyl octyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51323-70-7

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51323-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51323-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,2 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51323-70:
(7*5)+(6*1)+(5*3)+(4*2)+(3*3)+(2*7)+(1*0)=87
87 % 10 = 7
So 51323-70-7 is a valid CAS Registry Number.

51323-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-methylpropan-2-yl)oxy]octane

1.2 Other means of identification

Product number -
Other names 1-tert-butoxy-octane

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:51323-70-7 SDS

51323-70-7Relevant academic research and scientific papers

The rapid synthesis of organic compounds in microwave ovens. II

Gedye, Richard N.,Rank, Werner,Westaway, Kenneth

, p. 706 - 711 (2007/10/02)

Using microwaves to carry out organic reactions does not significantly alter the product composition.The small changes in product composition that are observed when microwaves are used arise because the microwave reactions occur at higher temperatures than reflux reactions.The results demonstrate that ions in the reaction mixture alter the heating rate of the microwave reactions.Although scaling-up the reaction leads to slightly lower rate reaction (lower percentage yield), one still retains large rate enhancements.

ALKYLATIONS EN ABSENCE DE SOLVANT ORGANIQUE-3. PREPARATION D'ETHERS ALIPHATIQUES PAR ALKYLATION DES ALCOOLATES DANS DES CONDITIONS DOUCES ET ECONOMIQUES.

Barry, J.,Bram, G.,Decodts, G.,Loupy, A.,Pigeon, P,Sansoulet, J.

, p. 2945 - 2950 (2007/10/02)

n-Octyl ethers are obtained by reacting n-octyl halides with performed alkoxides, or better, prepared in situ from ROH and solid KOH.Reactions are performed without any solvent but in the presence of a catalytic amount of tetra-alkyl ammonium salt (Aliquat 366).Good yields (>=92percent for primary R) are obtained at moderate temperatures and with easy work up; for t-C4H9O, elimination is a side reaction, and the effects of temperature and of the nature of the leaving group were examined, so that t-C4H9OC8H17 could then be obtained (yield 77percent) within 20 h at 36 deg C from n-octyl tosylate.

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