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33081-37-7

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33081-37-7 Usage

General Description

(βS,2R,5S)-β,5-Dimethyl-5β-vinyltetrahydrofuran-2β-ethanol, also known as vetiverol, is a chemical compound with a complex molecular structure. It is a natural product found in certain plants, particularly the roots of vetiver grass. Vetiverol is known for its unique aroma, which is often described as woody, earthy, and slightly sweet. It is commonly used in perfumery and fragrance products due to its pleasant scent. Additionally, vetiverol has been studied for its potential pharmacological properties, including anti-inflammatory and anti-cancer effects. Overall, this compound has both industrial and medicinal applications, making it an interesting subject of research in multiple fields.

Check Digit Verification of cas no

The CAS Registry Mumber 33081-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,8 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33081-37:
(7*3)+(6*3)+(5*0)+(4*8)+(3*1)+(2*3)+(1*7)=87
87 % 10 = 7
So 33081-37-7 is a valid CAS Registry Number.

33081-37-7SDS

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 lilac alcohol D

1.2 Other means of identification

Product number -
Other names -

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:33081-37-7 SDS

33081-37-7Downstream Products

33081-37-7Relevant articles and documents

INTRAMOLECULAR REACTIONS OF ALLYLOXY RADICALS

Johns, Amanda,Murphy, John A.,Sherburn, Michael S.

, p. 7835 - 7858 (2007/10/02)

Allyloxy radicals formed by epoxide cleavage, have cyclised onto appropriately positioned alkenes to form tetrahydrofurans, and the diastereoselectivity of the cyclisation has been studied.The reaction was used to synthesise lilac alcohols which were then used to confirm the stereochemistry of such cyclisations.

A HIGHLY STEREOSELECTIVE SYNTHESIS OF DAVANONE

Bartlett, Paul A.,Holmes, Christopher P.

, p. 1365 - 1368 (2007/10/02)

Iodocyclization of the anti 4-bromobenzyl ether acetate 4f is a key step in the first stereocontrolled synthesis of the trisubstituted tetrahydrofuran davanone.

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