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Cyclododecene, 1-methyl-, (1Z)-, also known as 1-methyl-1-cyclododecene, is an organic compound with the chemical formula C13H24. It is a colorless liquid with a strong, pungent odor. This cyclic alkene is characterized by a 12-carbon ring with a double bond between the first and second carbon atoms, and a methyl group attached to the first carbon. It is used as a fragrance ingredient in the perfume industry, as well as a chemical intermediate in the synthesis of various compounds. Due to its complex structure and unique properties, 1-methyl-1-cyclododecene is an important component in the creation of various scent profiles and chemical reactions.

4844-19-3

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4844-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4844-19-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4844-19:
(6*4)+(5*8)+(4*4)+(3*4)+(2*1)+(1*9)=103
103 % 10 = 3
So 4844-19-3 is a valid CAS Registry Number.

4844-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1-methylcyclododecene

1.2 Other means of identification

Product number -
Other names 1-Methylcyclododecene

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:4844-19-3 SDS

4844-19-3Upstream product

4844-19-3Relevant academic research and scientific papers

Reaction of Raney Nickel with Alcohols

Krafft, Marie E.,Crooks, William J.,Zorc, Branka,Milczanowski, Stephen E.

, p. 3158 - 3163 (2007/10/02)

The reaction of Raney nickel with a variety of functional groups was studied.Ethers, esters, and alkyl chlorides were found to be stable to Raney nickel in refluxing toluene; however, alcohols were found to be reactive.Primary alcohols were oxidized to aldehydes and the subsequently decarbonylated, secondary alcohols were oxidized to the corresponding ketone, and tertiary alcohols were deoxygenated.

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