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4-Hexen-1-ol, 5-methyl-2-(1-methylethylidene)-, also known as 5-methyl-2-(1-methylethylidene)hex-4-en-1-ol, is a naturally occurring organic compound with the molecular formula C10H18O. It is a colorless liquid with a strong, green, and herbaceous odor. This chemical is a member of the terpene family, which are a large and diverse group of organic compounds derived from isoprene units. It is commonly found in various plants, fruits, and vegetables, contributing to their distinct aromas. The compound is used in the fragrance industry as a natural alternative to synthetic fragrances, and it is also employed in the flavor industry to enhance the taste of food products. Due to its complex structure, it is often synthesized in laboratories for commercial use.

3304-27-6

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3304-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3304-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3304-27:
(6*3)+(5*3)+(4*0)+(3*4)+(2*2)+(1*7)=56
56 % 10 = 6
So 3304-27-6 is a valid CAS Registry Number.

3304-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methyl-2-(1'-methylethyliden)-4-hexen-1-ol

1.2 Other means of identification

Product number -
Other names 2-isopropylidene-5-methyl-hex-4-en-1-ol

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:3304-27-6 SDS

3304-27-6Relevant academic research and scientific papers

METHOD FOR PRODUCING 2-ISOPROPYLIDENE-5-METHYL-4-HEXENYL BUTYRATE

-

, (2015/05/05)

Provided is a simple and efficient method for producing 2-isopropylidene-5-methyl-4-hexenyl butyrate. More specifically, provided is a method for producing 2-isopropylidene-5-methyl-4-hexenyl butyrate, the method including the steps of: isomerizing 2-isopropenyl-5-methyl-4-hexenoic acid ester (1) into 2-isopropylidene-5-methyl-4-hexenoic acid ester (2), reducing thus formed 2-isopropylidene-5-methyl-4-hexenoic acid ester (2) into 2-isopropylidene-5-methyl-4-hexenol (3), and butyrylating thus formed 2-isopropylidene-5-methyl-4-hexenol (3) into 2-isopropylidene-5-methyl-4-hexenyl butyrate (4), wherein R represents a C1-10 hydrocarbon group.

Regio- and Stereoselective Synthesis of Allylic and Homoallylic Alcohols by the Reductive Desulfonylation of Allylic Sulfone Derivatives. Application to the Syntheses of (+/-)-Lavandulol and Isolavandulol

Inomata, Katsuhiko,Igarashi, Susumu,Mohri, Mitsunobu,Yamamoto, Taku,Kinoshita, Hideki,Kotake, Hiroshi

, p. 707 - 710 (2007/10/02)

Regio- and stereoselective desulfonylation of β-tosylhomoallylic alcohols provided a convenient method for the preparation of allylic and homoallylic alcohols. (+/-)-Lavandulol and isolavandulol were synthesized in excellent yields by this method.

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