Welcome to LookChem.com Sign In|Join Free
  • or
2,4-O-methylidenehexitol, a chemical compound with the molecular formula C7H14O5, is a derivative of hexitols, which are alcohols with six carbons and multiple hydroxyl groups. It is characterized by its unique chemical structure and reactivity, making it a versatile compound in various fields.

3013-59-0

Post Buying Request

3013-59-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3013-59-0 Usage

Uses

Used in Medicinal Chemistry and Pharmaceuticals:
2,4-O-methylidenehexitol is used as a precursor for the synthesis of various organic compounds, particularly in the field of medicinal chemistry and pharmaceuticals. Its unique structure and reactivity allow for the development of novel drug molecules with potential therapeutic applications.
Used in Carbohydrate-based Drug Molecules:
In the pharmaceutical industry, 2,4-O-methylidenehexitol serves as a building block for the preparation of carbohydrate-based drug molecules. Its ability to form stable glycosidic linkages with other molecules makes it an essential component in the design and synthesis of complex carbohydrate structures with medicinal properties.
Used in Flavor and Fragrance Ingredients:
2,4-O-methylidenehexitol is also utilized as an intermediate in the production of flavor and fragrance ingredients. Its unique chemical properties contribute to the creation of novel and diverse scents and tastes, enhancing the sensory experience in various consumer products.
Used in Material Science and Chemical Synthesis:
Due to its unique chemical structure and reactivity, 2,4-O-methylidenehexitol has potential applications in the areas of material science and chemical synthesis. It can be used to develop new materials with specific properties or as a key intermediate in the synthesis of other valuable compounds.
It is important to handle and use 2,4-O-methylidenehexitol with caution, as it may present hazards if not handled properly. Proper safety measures and guidelines should be followed to ensure the safe utilization of 2,4-O-methylidenehexitol in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3013-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,1 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3013-59:
(6*3)+(5*0)+(4*1)+(3*3)+(2*5)+(1*9)=50
50 % 10 = 0
So 3013-59-0 is a valid CAS Registry Number.

3013-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[5-hydroxy-6-(hydroxymethyl)-1,3-dioxan-4-yl]ethane-1,2-diol

1.2 Other means of identification

Product number -
Other names 2.4-O-Methylen-D-glucit

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:3013-59-0 SDS

3013-59-0Relevant academic research and scientific papers

Synthesis of carbohydrate containing crown ethers and their application as catalysts in asymmetric Michael additions

Van Maarschalkerwaart,Willard,Pandit

, p. 8825 - 8840 (2007/10/02)

Synthesis of carbohydrate containing crown ethers tuned with steric and micro-environmental features and thier application as catalysts in the Michael addition of methyl phenylacetate to methyl acrylate to give a chiral products is reported. The mechanistic rationale of the asymmetric induction is discussed.

Stereoselective formation of tetrahydrofurans during allyltrimethylsilane additions to L-xylose derivatives

Veloo, Ronald A.,Wanner, Martin J.,Koomen, Gerrit-Jan

, p. 5301 - 5316 (2007/10/02)

Stereoselective addition reactions to the aldehyde function of some L-xylose derivatives, under the influence of Lewis acid catalysts, lead to the formation of tetrahydrofuran derivatives at low temperatures, depending on the acetal protecting groups used

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3013-59-0