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Phosphonic acid, phenyl-, mono(1,1-dimethylethyl) ester, also known as tris(1,1-dimethylethyl) phenylphosphonite, is an organophosphorus compound with the chemical formula C15H25O2P. It is a colorless liquid with a molecular weight of 266.33 g/mol. Phosphonic acid, phenyl-, mono(1,1-dimethylethyl) ester is characterized by its phosphonic acid group attached to a phenyl ring and a single tert-butyl (1,1-dimethylethyl) ester group. It is used as a stabilizing agent, flame retardant, and intermediate in the synthesis of various organophosphorus compounds. Due to its chemical structure, it exhibits low toxicity and is considered environmentally friendly. It is widely used in the plastics, rubber, and coatings industries to enhance the stability and performance of materials.

7671-12-7

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7671-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7671-12-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,7 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7671-12:
(6*7)+(5*6)+(4*7)+(3*1)+(2*1)+(1*2)=107
107 % 10 = 7
So 7671-12-7 is a valid CAS Registry Number.

7671-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylpropan-2-yl)oxy-phenylphosphinate

1.2 Other means of identification

Product number -
Other names Phosphonic acid,phenyl-,mono(1,1-dimethylethyl) ester

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:7671-12-7 SDS

7671-12-7Downstream Products

7671-12-7Relevant academic research and scientific papers

Competition of methanol and tert-butanol in nucleophilic substitution at phosphorus atom

Cieplucha, Agnieszka,Jankowski, Stefan

experimental part, p. 1448 - 1453 (2010/03/24)

2,3-Oxaphosphabicyclo[2.2.2]octene 1 reacts with alcohols simultaneously according to two competitive mechanisms: bimolecular addition-elimination and unimolecular elimination-addition with the intermediacy of metaphosphonate Ph-PO2 (2). In 1,2-dichloroet

Regioselective formation of a 2,3-oxaphosphabicyclo[2.2.2] octene 3-oxide in baeyer-villiger type oxidation; a dual pathway for its fragmentation

Jankowski, Stefan,Kovacs, Janos,Huben, Krzysztof,Blaszczyk, Michal,Glowka, Marek,Keglevich, Gyoergy

, p. 369 - 375 (2007/10/03)

The O-insertion reaction of a 7-phosphanorbornene (3) unsubstituted on the double-bond gave the corresponding 2,3-oxaphosphabicyclo-[2.2.2]octene oxide (4a) in a regioselective manner that was useful in the fragmentation-related phosphonylation of alcohol

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