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(METHOXYMETHYL)-CYCLOPENTANE, also known as a cyclopentane derivative, is a chemical compound characterized by a cyclopentane ring with a methoxymethyl group attached to one of its carbon atoms. This group, derived from methanol, is commonly utilized as a protecting group in organic synthesis. (METHOXYMETHYL)-CYCLOPENTANE is a colorless liquid with a mild, sweet odor and is recognized for its versatility in the synthesis of various organic compounds.

2619-30-9

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2619-30-9 Usage

Uses

Used in Industrial Solvents:
(METHOXYMETHYL)-CYCLOPENTANE is used as an industrial solvent due to its ability to dissolve a wide range of substances, making it a valuable component in various manufacturing processes.
Used in Organic Chemistry:
In the field of organic chemistry, (METHOXYMETHYL)-CYCLOPENTANE serves as a reagent, playing a crucial role in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
(METHOXYMETHYL)-CYCLOPENTANE is used as a building block in the production of pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemicals:
(METHOXYMETHYL)-CYCLOPENTANE is also utilized in the agrochemical industry, where it is employed in the synthesis of various chemicals used in agriculture.
Used in Fragrance and Flavor Manufacturing:
(METHOXYMETHYL)-CYCLOPENTANE has applications in the manufacturing of fragrance and flavor compounds, capitalizing on its mild, sweet odor to create appealing scents and tastes for the consumer market.

Check Digit Verification of cas no

The CAS Registry Mumber 2619-30-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2619-30:
(6*2)+(5*6)+(4*1)+(3*9)+(2*3)+(1*0)=79
79 % 10 = 9
So 2619-30-9 is a valid CAS Registry Number.

2619-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methoxymethylcyclopentane

1.2 Other means of identification

Product number -
Other names (Methoxymethyl)-cyclopentane

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:2619-30-9 SDS

2619-30-9Downstream Products

2619-30-9Relevant academic research and scientific papers

Kinetics and mechanism of the aminolysis of cycloalkylmethyl arenesulfonates

Oh, Hyuck Keun,Song, Se Jeong,Jo, Dong-Soo,Lee, Ikchoon

, p. 91 - 96 (2007/10/03)

Nucleophilic substitution reactions of cycloalkylmethyl arenesulfonates (CmH2n-1 CH2OSO2C6H4Z) with anilines (XC6H4NH2) in methanol at 65.0 °C were studied. The reactivity order (n=4>6>7>5) reflects largely the order of steric effect of the ring size (SEs term) except for n=5, which exhibits the least reactivity. This reversal of the order for n=5 is considered to result from large rate retardation due to polar effect of the ρ*σ* term. Application of the Taft equation to the rate data for n=5 and 6 gives ρ=17·4 and 5=2·3 with correlation coefficient of 0·90. The σ* values for n=4 and 7 are estimated to be - 0·23 and - 0·11, respectively. The positive ρxz values of ca 0·3 are consistent with previous results for the reactions at primary reaction centers.

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