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Phosphonic acid, (3,7-dimethyl-6-octenyl)-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25901-59-1

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25901-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25901-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,0 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25901-59:
(7*2)+(6*5)+(5*9)+(4*0)+(3*1)+(2*5)+(1*9)=111
111 % 10 = 1
So 25901-59-1 is a valid CAS Registry Number.

25901-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-diethoxyphosphoryl-2,6-dimethyloct-2-ene

1.2 Other means of identification

Product number -
Other names diethyl 3,7-dimethyl-6-octenylphosphonate

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:25901-59-1 SDS

25901-59-1Downstream Products

25901-59-1Relevant academic research and scientific papers

Three-Component Coupling of Acylphosphonates and Two Carbonyl Compounds Promoted by Low-Valent Samariums: One-Pot Synthesis of β-Hydroxyphosphonates

Takaki, Ken,Itono, Yuichiro,Nagafuji, Akihiro,Naito, Yoji,Shishido, Tetsuya,Takehira, Katsuomi,Makioka, Yoshikazu,Taniguchi, Yuki,Fujiwara, Yuzo

, p. 475 - 481 (2007/10/03)

Three-component coupling of acylphosphonates and two carbonyl compounds leading to β-hydroxyphosphonates has been achieved with low-valent samariums. Thus, acylphosphonates reacted with aldehydes in the presence of semicatalytic amounts of samarium metal or SmI2 to give acyloxyphosphonates in good yields. The second coupling reaction of the acyloxyphosphonates with aldehydes or ketones promoted by SmI2 afforded β-hydroxyphosphonates instead of olefins. Moreover, these two reactions could be carried out in one pot.

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