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3013-59-0

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3013-59-0 Usage

General Description

2,4-O-methylidenehexitol is a chemical compound with the molecular formula C7H14O5. It is a derivative of hexitols, which are alcohols with six carbons and multiple hydroxyl groups. 2,4-O-methylidenehexitol is most commonly used as a precursor for the synthesis of various organic compounds, particularly in the field of medicinal chemistry and pharmaceuticals. It is also utilized as a building block for the preparation of carbohydrate-based drug molecules and as an intermediate in the production of flavor and fragrance ingredients. Additionally, it has potential applications in the areas of material science and chemical synthesis due to its unique chemical structure and reactivity. However, it is important to handle and use 2,4-O-methylidenehexitol with caution, as it may present hazards if not handled properly.

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 articles and documents

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.

Syntheses and cytotoxicity of the AB-, C-, and BC-ring systems of sesbanimides

Matsuda,Ohsaki,Yamada,Terashima

, p. 2123 - 2131 (2007/10/02)

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