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2619-30-9

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2619-30-9 Usage

General Description

(Methoxymethyl)-cyclopentane is a chemical compound that consists of a cyclopentane ring with a methoxymethyl group attached to one of its carbon atoms. The methoxymethyl group is derived from methanol and is often used as a protecting group in organic synthesis. (METHOXYMETHYL)-CYCLOPENTANE is a colorless liquid with a mild, sweet odor and is primarily used as an industrial solvent and as a reagent in organic chemistry. It is also used in the production of pharmaceuticals and agrochemicals. Additionally, (methoxymethyl)-cyclopentane has applications in the manufacturing of fragrance and flavor compounds. Overall, this chemical serves as a versatile building block in the synthesis of various organic compounds and has several industrial and commercial uses.

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 articles and documents

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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