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Furan, 3-methyl-2-(3-methyl-3-butenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17290-68-5

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17290-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17290-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,9 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17290-68:
(7*1)+(6*7)+(5*2)+(4*9)+(3*0)+(2*6)+(1*8)=115
115 % 10 = 5
So 17290-68-5 is a valid CAS Registry Number.

17290-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2-(3-methylbut-3-enyl)furan

1.2 Other means of identification

Product number -
Other names Isorosenfuran

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:17290-68-5 SDS

17290-68-5Downstream Products

17290-68-5Relevant academic research and scientific papers

A Practical Synthesis of Rosefuran. Furans from Acetylenes and Allyl Alcohols

Trost, Barry M.,Flygare, John A.

, p. 1078 - 1082 (1994)

A new atom-economical synthetic strategy for the synthesis of furans emerges from β,γ-unsaturated ketones which are readily available from acetylenes and allyl alcohols by simple additions in the presence of a ruthenium catalyst.Dihydroxylation using cata

Reaction of Carboxonium Ions of Cyclic Acetals, IX. - Synthesis of Rosefuran and Structurally Related Terpene-like Esters, Alcohols, and Olefins

Meier, Lothar,Scharf, Hans-Dieter

, p. 731 - 740 (2007/10/02)

Thermolysis of the 4-(o-toluoyloxy)-1,3-dioxolanes 4 leads to the furans 6/7 which, via Grignard reaction, can be converted into the alcohols 8/9.Subsequent dehydratization affords the olefins 10/11, e.g. rosefuran (10a).

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