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158817-45-9

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158817-45-9 Usage

General Description

(3S)-1,3-Dioxane-2-methyl-4-carboxylic acid is a chemical compound with a molecular formula C7H12O4. It is a carboxylic acid derivative that contains a dioxane ring and a methyl group. (3S)-1,3-DIOXANE-2-METHYL-4-CARBOXYLIC ACID is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and organic compounds. It has also been studied for its potential antimicrobial and antioxidant properties. Additionally, (3S)-1,3-dioxane-2-methyl-4-carboxylic acid has been found to have potential applications in the field of medicinal chemistry and drug discovery due to its unique structure and potential biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 158817-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,8,1 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 158817-45:
(8*1)+(7*5)+(6*8)+(5*8)+(4*1)+(3*7)+(2*4)+(1*5)=169
169 % 10 = 9
So 158817-45-9 is a valid CAS Registry Number.

158817-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,4S)-2-methyl-1,3-dioxane-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:158817-45-9 SDS

158817-45-9Downstream Products

158817-45-9Relevant articles and documents

Reductive Lithiation of Alkyl 2-Thiopyridyl Ethers to Generate Optically Pure α-Alkoxylithium Reagents

Rychnovsky, Scott D.,Plzak, Kevin,Pickering, Dacia

, p. 6799 - 6802 (1994)

Enantiomerically pure 4-lithio-2-alkyl-1,3-dioxanes, 11 and 13 were prepared by reductive lithiation of alkyl 2-thiopyridyl ether 10, which was in turn prepared by Barton radical decarboxylation of the homogenous acid.The optical activity was introduced by chirality transfer to and from the stereogenic acetal center. - Keywords - reductive lithiation; acetals; chirality transfer; thiopyridyl; radical decarboxylation.

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