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129228-07-5

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129228-07-5 Usage

General Description

4,4-bis(methoxymethyl)-2,6-dimethylheptane is a specific structural isomer of heptane, a hydrocarbon with the formula C7H16. This particular compound has additional methyl (CH3) and methoxymethyl (CH2OCH3) groups branching off the main heptane chain. This arrangement results in a molecule characterized by increased complexity and molecular weight compared to standard heptane. The properties, reactivity, and applications of 4,4-bis(methoxymethyl)-2,6-dimethylheptane will depend on the nature of these substituents and their influence on the molecular structure as a whole. Unfortunately, this compound is not well-studied, so specific details about its behavior, toxicity, or potential uses are not readily available.

Check Digit Verification of cas no

The CAS Registry Mumber 129228-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,2,2 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129228-07:
(8*1)+(7*2)+(6*9)+(5*2)+(4*2)+(3*8)+(2*0)+(1*7)=125
125 % 10 = 5
So 129228-07-5 is a valid CAS Registry Number.

129228-07-5SDS

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 4,4-bis(methoxymethyl)-2,6-dimethylheptane

1.2 Other means of identification

Product number -
Other names 2,2-di-i-butyl-1,3-dimethoxypropane

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:129228-07-5 SDS

129228-07-5Synthetic route

2,2-di-i-butyl-1,3-dimethoxypropane
129228-07-5

2,2-di-i-butyl-1,3-dimethoxypropane

titanium tetrachloride
7550-45-0

titanium tetrachloride

μ-oxo-bis{trichloro(2,2-diisobutyl-1,3-dimethoxypropane-O,O')titanium(IV)}

μ-oxo-bis{trichloro(2,2-diisobutyl-1,3-dimethoxypropane-O,O')titanium(IV)}

Conditions
ConditionsYield
With air; water In n-heptane reaction of TiCl4 and the ligand in n-heptane gives the monomeric intermediate which is converted to the product by standing in moist air;
2,2-di-i-butyl-1,3-dimethoxypropane
129228-07-5

2,2-di-i-butyl-1,3-dimethoxypropane

magnesium ethylate
2414-98-4

magnesium ethylate

titanium tetrachloride
7550-45-0

titanium tetrachloride

solid catalyst component

solid catalyst component

Conditions
ConditionsYield
Stage #1: magnesium ethylate; titanium tetrachloride In toluene at 5℃; for 1h;
Stage #2: 2,2-di-i-butyl-1,3-dimethoxypropane In toluene at 100℃; for 2h;
Stage #3: titanium tetrachloride In toluene at 110℃; for 2h;

129228-07-5Upstream product

129228-07-5Downstream Products

129228-07-5Relevant articles and documents

Diethers usable in the preparation of Ziegler-Natta catalysts and their preparation

-

, (2008/06/13)

Diethers of general formula: where R, RI, RII, RIII, RIVand RV, same or different, are H or linear or branched alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl radicals with 1-18 carbon atoms, provided that R and RIare not both H or CH3 or are not CH3 and n-propyl; RVIand RVIIthe same or different, are linear or branched alkyl, cycloaliphatic, aryl, or arylalkyl radicals having 1-18 carbon atoms; one or more of R to RVIImay be bonded to form a cyclic structure. The diethers are particularly useful in the preparation of Ziegler-Natta catalysts.

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