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1,3-Dithiane, 2-[4-methoxy-3-(phenylmethoxy)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57009-78-6

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57009-78-6 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

A dithiane derivative is a compound that contains a dithiane ring, which is a six-membered ring containing two sulfur atoms.

Explanation

The compound is commonly used in organic synthesis to protect aldehyde and ketone functional groups from unwanted reactions.

Explanation

The compound is a solid at room temperature and has a yellow color.

Explanation

The compound can dissolve in organic solvents, which is important for its use in organic synthesis.

Explanation

The compound is utilized in the synthesis of complex organic molecules, which are essential in various fields, including pharmaceuticals and fine chemicals.

Explanation

The compound plays a significant role in the development of various pharmaceuticals due to its ability to protect carbonyl groups during synthesis.

Explanation

The unique chemical properties of the compound make it a valuable reagent in organic chemistry, particularly for protecting carbonyl groups during reactions.

Dithiane Derivative

Yes

Use as a Protecting Group

Aldehydes and Ketones

Physical State

Yellow Solid

Solubility

Soluble in Organic Solvents

Application

Formation of Complex Organic Molecules

Role in Pharmaceutical Development

Crucial

Chemical Properties

Valuable Reagent for Carbonyl Group Protection

Check Digit Verification of cas no

The CAS Registry Mumber 57009-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,0 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57009-78:
(7*5)+(6*7)+(5*0)+(4*0)+(3*9)+(2*7)+(1*8)=126
126 % 10 = 6
So 57009-78-6 is a valid CAS Registry Number.

57009-78-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxy-3-phenylmethoxyphenyl)-1,3-dithiane

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:57009-78-6 SDS

57009-78-6Relevant academic research and scientific papers

Synthesis and cytotoxic activities of 4,5-diarylisoxazoles

Sun, Chang-Ming,Lin, Lee-Gin,Yu, Hsi-Jung,Cheng, Chih-Yu,Tsai, Ya-Chuan,Chu, Chi-Wei,Din, Yi-Hui,Chau, Yat-Pang,Don, Ming-Jaw

, p. 1078 - 1081 (2007)

A series of 4,5-diarylisoxazoles related to combretastatin A-4 (CA-4) were synthesized and evaluated for cytotoxicity against three human cancer cell lines. Among them, compound 6e showed better cytotoxic activity than CA-4 in HeLa and HepG2 cell lines as

Preparing method of 2-substituted-1,3-dithiane derivative

-

Paragraph 0020-0026; 0060-0062, (2018/10/02)

The invention belongs to the technical field of organic synthesis, and particularly discloses a preparing method of a 2-substituted-1,3-dithiane derivative. The preparing method comprises the following steps of adding substrate aldehyde, 1,3-dimercaptopro

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