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1,3-Propanediol,2-[(2-methyl-1,3-dithian-2-yl)methyl]-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

798550-49-9

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798550-49-9 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 7 carbon (C), 16 hydrogen (H), 2 oxygen (O), and 2 sulfur (S) atoms.

Explanation

The compound is derived from 1,3-propanediol, which is a diol with two hydroxyl (OH) groups. It has an additional 2-methyl-1,3-dithian-2-yl)methyl group attached to it, which is a sulfur-containing organic compound.

Explanation

As the compound contains two hydroxyl groups, it is classified as a diol, which is a type of alcohol with two hydroxyl groups.

Explanation

The 2-methyl-1,3-dithian-2-yl)methyl group in the compound contributes to its sulfur content, making it a sulfur-containing organic compound.

Explanation

Due to its unique structure and functional groups, the compound is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals.

Explanation

The specific physical properties of the compound, such as melting point, boiling point, and solubility, may vary depending on its intended use and the conditions under which it is synthesized or processed.

Explanation

As a synthetic organic compound, it is generally stable under normal conditions, such as room temperature and pressure. However, its stability may be affected by factors like temperature, light, and exposure to air or moisture.

Chemical Structure

1,3-Propanediol with a 2-methyl-1,3-dithian-2-yl)methyl group

Functional Groups

Two hydroxyl groups, 1,3-dithiane ring, and a methyl group

Classification

Diol compound

Sulfur Content

Contains sulfur

Applications

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Physical Properties

May vary depending on the application

Stability

Generally stable under normal conditions

Hazards

Potential hazards may include toxicity, flammability, or reactivity with other chemicals

Check Digit Verification of cas no

The CAS Registry Mumber 798550-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,8,5,5 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 798550-49:
(8*7)+(7*9)+(6*8)+(5*5)+(4*5)+(3*0)+(2*4)+(1*9)=229
229 % 10 = 9
So 798550-49-9 is a valid CAS Registry Number.

798550-49-9SDS

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 2-(2-Methyl-[1,3]dithian-2-ylmethyl)-propane-1,3-diol

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:798550-49-9 SDS

798550-49-9Downstream Products

798550-49-9Relevant academic research and scientific papers

Enzyme assisted syntheses of chiral building blocks for isosters of diglycerides, phospholipids and PAF

Lange, Karsten,Schneider, Manfred P.

, p. 2811 - 2815 (2007/10/03)

Lipase catalyzed desymmetrizations of suitably substituted, achiral 1,3-diols lead to the corresponding chiral building blocks of high enantiomeric purities, starting materials for the synthesis of isosteric carba-analogues of 1,2-sn-diglycerides and phospholipids with interesting biological activities. Lipase catalyzed resolutions of the corresponding ether derivatives lead to the corresponding building blocks for carba-analogues of PAF.

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