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1-[(2-Hydroxyethyl)thio]propan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6713-03-7

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6713-03-7 Usage

Chemical Properties

Colorless Oil

Uses

Hydroxyethylthio Propanol (cas# 6713-03-7) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 6713-03-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6713-03:
(6*6)+(5*7)+(4*1)+(3*3)+(2*0)+(1*3)=87
87 % 10 = 7
So 6713-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H12O2S/c1-5(7)4-8-3-2-6/h5-7H,2-4H2,1H3

6713-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Hydroxyethylthio Propanol

1.2 Other means of identification

Product number -
Other names 1-(2-hydroxyethylsulfanyl)propan-2-ol

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:6713-03-7 SDS

6713-03-7Relevant academic research and scientific papers

Efficient synthesis of β, β'-dihydroxy sulfides by ring opening of epoxides with mercaptoethanol catalyzed under solvent-free conditions

Romdhani-Younes, Moufida,Chaabouni, Mohamed Moncef

experimental part, p. 223 - 228 (2012/05/31)

A simple and highly efficient synthesis of β, β′-dihydroxy sulfides has been achieved by ring opening of epoxides with mercaptoethanol using catalytic amount of benzyltrimethylammonium hydroxide (Triton B) under solvent-free conditions. Excellent regioselectivity was found for aliphatic unsymmetrical epoxides, with nucleophilic attack at the less-hindered carbon atom of the epoxide. However, this regioselectivitywas not observed for styrene oxide and a mixture of two isomers was obtained. This process was also regio- and chemo-selective as illustrated using epichlorohydrin with two epoxide ring positions and mercaptoethanol with two functional groups (SH and OH). Figure Presented.

N-AMINO TETRAHYDROTHIAZINE DERIVATIVES, METHOD OF MANUFACTURE AND USE

-

Page/Page column 18, (2008/12/07)

This invention comprises the innovative synthesis of N-amino tetrahydrothiazine free bases and their salts. This invention further comprises the use of the derivatives and their therapeutic application as anticancer agents. Further this invention comprises their manufacture and use.

NITROFURAN COMPOUNDS FOR THE TREATMENT OF CANCER AND ANGIOGENESIS

-

Page/Page column 48-49, (2008/06/13)

The invention is directed to the synthesis and use of nitrofuran compounds, especially Nifurtimox, as medicaments to treat cancer, especially neuroblastoma, and to inhibit angiogenesis. The invention also provides compositions, unit dosage forms, and kits comprising the compounds.

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