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2-methylbutan-2-yl chloroacetate is an organic compound with the chemical formula C7H13ClO2. It is a colorless liquid with a molecular weight of 160.63 g/mol. 2-methylbutan-2-yl chloroacetate is derived from 2-methylbutan-2-ol, where the hydroxyl group is replaced by a chloroacetyl group. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is characterized by its reactivity, as the chloroacetyl group can undergo nucleophilic substitution reactions, making it a valuable building block in organic synthesis. It is also known for its potential applications in the preparation of chiral auxiliaries and ligands in asymmetric catalysis. Due to its reactivity and versatility, 2-methylbutan-2-yl chloroacetate is an important compound in the field of organic chemistry.

5439-30-5

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5439-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5439-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5439-30:
(6*5)+(5*4)+(4*3)+(3*9)+(2*3)+(1*0)=95
95 % 10 = 5
So 5439-30-5 is a valid CAS Registry Number.

5439-30-5SDS

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 2-methylbutan-2-yl 2-chloroacetate

1.2 Other means of identification

Product number -
Other names 2-methylbut-2-yl chloroacetate

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:5439-30-5 SDS

5439-30-5Relevant academic research and scientific papers

Novel lactonization of ethenetricarboxylate derivatives: Intermolecular trapping of alkenes

Yamazaki, Shoko,Ohmitsu, Kanae,Ohi, Kunihiro,Otsubo, Tetsuya,Moriyama, Kayo

, p. 759 - 762 (2007/10/03)

(Chemical Equation Presented) A novel cyclization of 1,1-diethyl 2-tert-butyl ethenetricarboxylate (1a) in the presence of a Lewis acid afforded a 5,5-dimethyl-γ-lactone derivative 2a. The reaction process has been shown to arise from formation by trappin

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