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Tetrahydrofuran-2-ylmethyl 2,2-dimethylpropanoate is a complex organic compound with the chemical formula C10H18O3. It is a derivative of tetrahydrofuran, a cyclic ether, and 2,2-dimethylpropanoic acid, a branched-chain carboxylic acid. tetrahydrofuran-2-ylmethyl 2,2-dimethylpropanoate is characterized by a tetrahydrofuran ring attached to a 2,2-dimethylpropanoate group, which is a three-carbon chain with two methyl groups attached to the central carbon. It is a colorless liquid with a low boiling point and is insoluble in water. Due to its unique structure, it is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds.

7461-07-6

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7461-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7461-07-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7461-07:
(6*7)+(5*4)+(4*6)+(3*1)+(2*0)+(1*7)=96
96 % 10 = 6
So 7461-07-6 is a valid CAS Registry Number.

7461-07-6SDS

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 oxolan-2-ylmethyl 2,2-dimethylpropanoate

1.2 Other means of identification

Product number -
Other names TETRAHYDROFURAN-2-YLMETHYL 2,2-DIMETHYLPROPANOATE

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:7461-07-6 SDS

7461-07-6Downstream Products

7461-07-6Relevant academic research and scientific papers

Processes for preparation of nucleoside derivatives

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, (2008/06/13)

Improved processes for production of useful nucleoside derivatives of formula (VI) wherein B1 is a pyrimidinyl group of Formula XXI or a purinyl group of Formula XXII, in which V is amino or hydroxy,R2 is hydrogen or methyl, and, R3 is hydrogen or amino;

Tetrahydrofuran intermediates

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, (2008/06/13)

Novel tetrahydrofuran and dihydrofuran derivatives useful as synthetic chemical intermediates and processes for their preparation.

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