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62987-01-3

62987-01-3

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62987-01-3 Usage

Chemical Properties

clear colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 62987-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,8 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62987-01:
(7*6)+(6*2)+(5*9)+(4*8)+(3*7)+(2*0)+(1*1)=153
153 % 10 = 3
So 62987-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-2-3-6-9-8-5-4-7-10-8/h8H,2-7H2,1H3/t8-/m0/s1

62987-01-3SDS

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 2-butoxyoxolane

1.2 Other means of identification

Product number -
Other names 2-BUTOXYTETRAHYDROFURAN

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:62987-01-3 SDS

62987-01-3Downstream Products

62987-01-3Relevant articles and documents

Environmentally friendly tetrahydrofuranylation of alcohols using NaHSO4SiO2 under solvent-free conditions

Kinfe, Henok H.,Terblanche, Sullivan,Tshivhase, Konanani D.,Ravhura, Livhuwani

experimental part, p. 272 - 273 (2012/05/20)

A simple, environmentally friendly, and efficient tetrahydrofuranylation of alcohols has been developed using NaHSO4SiO2 (0.5 mol%) as a catalyst under solvent-free conditions to yield corresponding THF ethers in good to excellent yi

Synthesis of 2-tetrahydrofuranyl ethers from aqueous 4-hydroxybutanal

Lawson,Klang

, p. 3205 - 3210 (2007/10/02)

2-Tetrahydrofuranyl ethers are prepared simply and in high yield from an alcohol and aqueous 4-hydroxybutanal using a two phase reaction system.

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