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2,2'-(decamethylenedithio)diethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6964-20-1

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6964-20-1 Usage

Originator

Fonlipol,Lafon,France,1972

Manufacturing Process

Thioethylene glycol, HSCH2CH2OH (prepared from ethylene oxide and hydrogen sulfide) is first reacted with sodium to give HOCH2CH2SNa.It is then reacted with decamethylene bromide, Br(CH2)10Br to give tiadenol.

Therapeutic Function

Antihyperlipidemic

Check Digit Verification of cas no

The CAS Registry Mumber 6964-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6964-20:
(6*6)+(5*9)+(4*6)+(3*4)+(2*2)+(1*0)=121
121 % 10 = 1
So 6964-20-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H30O2S2/c15-9-13-17-11-7-5-3-1-2-4-6-8-12-18-14-10-16/h15-16H,1-14H2

6964-20-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol

1.2 Other means of identification

Product number -
Other names LL 1558

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:6964-20-1 SDS

6964-20-1Downstream Products

6964-20-1Relevant academic research and scientific papers

SYNTHESIS OF TELECHELIC MONODISPERSED DIOLS. PART 3. TELOMERIZATION OF NONCONJUGATED DIENES WITH COMMERCIALLY AVAILABLE OR SYNTHESIZED MERCAPTO-ALCOHOLS

Ameduri, Bruno,Berrada, Khalid,Boutevin, Bernard,Bowden, Roy D.

, p. 39 - 48 (2007/10/02)

The synthesis of telechelic monodispersed diols produced from the radical telomerization of commercially available nonconjugated dienes (1,5-hexadiene and 1,9-decadiene) with an excess of commercial (2-mercapto-ethanol) or synthesized thio-alcohol, initiated by peroxydes is presented.In each case, the diols were obtained selectively and in excellent yields and were characterized by both 1H and 13C-NMR.The thermostability of these latter diols is much better than that of polydispersed commercially available diols such as polyethylene glycol or poly(THF).Key words:Telechelic diol; monodispersity; radical telomerization; mercapto-alcohol; thermostability.

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