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(4Z)-2,2,7,7-tetramethyloct-4-ene is an organic compound with the molecular formula C12H24. It is a colorless liquid with a strong, pungent odor. This alkene features a double bond between the 4th and 5th carbon atoms, with four methyl groups attached to the 2nd, 2nd, 7th, and 7th carbon atoms, respectively. The compound is known for its high reactivity due to the presence of the double bond, which can undergo various chemical reactions such as addition, polymerization, and oxidation. It is commonly used in the synthesis of various organic compounds and as a precursor in the production of fragrances, pharmaceuticals, and other specialty chemicals.

5223-57-4

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5223-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5223-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5223-57:
(6*5)+(5*2)+(4*2)+(3*3)+(2*5)+(1*7)=74
74 % 10 = 4
So 5223-57-4 is a valid CAS Registry Number.

5223-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-2,2,7,7-tetramethyloct-4-ene

1.2 Other means of identification

Product number -
Other names cis-2,2,7,7-Tetramethyl-4-octene

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:5223-57-4 SDS

5223-57-4Upstream product

5223-57-4Downstream Products

5223-57-4Relevant academic research and scientific papers

Secondary isotope effects in dioxirane epoxidations. Concerted or step-wise mechanism?

Angelis, Yiannis,Zhang, Xiaojun,Orfanopoulos, Michael

, p. 5991 - 5994 (1996)

The inverse α- and β-secondary isotope effects found for the epoxidation reaction of dimethyl dioxirane (DMD) with alkenes support a non polar concerted mechanism.

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