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627-02-1

627-02-1

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627-02-1 Usage

Uses

Isobutyl Ethyl Ether was identified in the biopreservation system formed by coupling Lactobacillus reuteri INIA P572 and glycerol.

Check Digit Verification of cas no

The CAS Registry Mumber 627-02-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 627-02:
(5*6)+(4*2)+(3*7)+(2*0)+(1*2)=61
61 % 10 = 1
So 627-02-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O/c1-4-7-5-6(2)3/h6H,4-5H2,1-3H3

627-02-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ETHOXY-2-METHYLPROPANE

1.2 Other means of identification

Product number -
Other names oxyethylene mono-isobutyl ether

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:627-02-1 SDS

627-02-1Relevant articles and documents

-

Mailhe,de Godon

, p. 123-126, 329 (1920)

-

Deamination Reactions, 41. Reactions of Aliphatic Diazonium Ions and Carbocations with Ethers

Kirmse, Wolfgang,Jansen, Ulrich

, p. 2607 - 2625 (2007/10/02)

Aliphatic diazonium ions and carbocations were generated by deacylation of appropriate nitrosoureas (1, 5, 9) in alcohol-ether mixtures or in 2-alkoxyethanols.Ethers were generally inferior to alcohols in capturing cationic intermediates.Formation of trialkyloxonium ions led to alkyl exchange or ring opening.The observed reactivity orders were n-butyl > isobutyl for the diazonium ions, allyl > sec-butyl > tert-butyl for the carbocations, methoxy > ethoxy and oxirane > oxetane > tetrahydrofuran for the ethers, indicating the predominance of steric effects.Neighboring group participation in 4-methoxy-1-butanediazonium ions (58) and 4,5-epoxy-1-pentanediazonium ions (74) was detectable but inefficient ( 20percent of cyclic oxonium ions).

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