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Furan, tetrahydro-2-methyl-5-(1-methylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50551-99-0

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50551-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50551-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,5 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50551-99:
(7*5)+(6*0)+(5*5)+(4*5)+(3*1)+(2*9)+(1*9)=110
110 % 10 = 0
So 50551-99-0 is a valid CAS Registry Number.

50551-99-0SDS

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-(1-methylvinyl)-5-methyl-tetrahydrofuran

1.2 Other means of identification

Product number -
Other names 2-isopropenyl-5-methyl-tetrahydro-furan

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:50551-99-0 SDS

50551-99-0Downstream Products

50551-99-0Relevant academic research and scientific papers

Reaction of some alkenols with tetrachloromethane

Bugarcic, Zorica M.,Mojsilovic, Biljana,Marjanovic, Ljiljana,Konstantinovic, Stanimir

, p. 1091 - 1096 (2007/10/03)

The reaction of some alkenols with tetrachloromethane in the presence of a radical initiator was investigated. Regarding the effects of structural features of the starting alkenol (number and position of methyl substituents at the double bond and at the carbinol carbon atom, constitutional relationship between the double bond and the hydroxyl group) there are two possible competing reactions: addition and cyclization. In the case of the simplest alkenols (without substituents and with a more remote double bond) addition occurs; mono-and disubstituted secondary and tertiary Δ4-and Δ5-alkenols cyclize in high yields to give the corresponding cyclic ethers.

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