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2-Cyclododecen-1-ol, (E)-, also known as cis-2-cyclododecen-1-ol, is a naturally occurring organic compound with a molecular formula of C12H22O. It is a cyclododecenol, which means it has a 12-carbon cyclic structure with a hydroxyl group attached to the first carbon. 2-Cyclododecen-1-ol, (E)- is characterized by its distinct, musky odor and is commonly found in various essential oils, such as those derived from flowers and plants. It is used in the fragrance industry as a fixative and in the production of perfumes, due to its ability to enhance and stabilize the scent of other compounds. Additionally, 2-cyclododecen-1-ol, (E)-, has been identified as a pheromone in some insects, playing a crucial role in their communication and mating behaviors.

6221-49-4

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6221-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6221-49-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6221-49:
(6*6)+(5*2)+(4*2)+(3*1)+(2*4)+(1*9)=74
74 % 10 = 4
So 6221-49-4 is a valid CAS Registry Number.

6221-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2-cyclododecen-1-ol

1.2 Other means of identification

Product number -
Other names (E)-cyclododec-2-enol

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:6221-49-4 SDS

6221-49-4Upstream product

6221-49-4Relevant academic research and scientific papers

Isomerization of Cyclooctene and Cyclododecene Oxides Catalyzed by Solid Acids and Bases

Arata, Kazushi,Nakamura, Hideo,Nakamura, Yuki

, p. 2351 - 2353 (1994)

The title reactions were carried out over seven catalysts.From cyclooctene oxide a large amount of 7-octenal was formed together with 3-cycloocten-1-ol over SiO2-Al2O3 and SiO2-TiO2, 3-cycloocten-1-ol over solid H3PO4, and cyclooctanone over FeSO4.Most catalysts except for NiSO4, Al2O3, and Tio2-ZrO2 produced 1,3-cyclododecadiene, cyclododecanone, and 2-cyclododecen-1-ol uniformly from cyclododecene oxide.Allylic alcohols were preferentially given by Al2O3 and TiO2-ZrO2.

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