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2,2,2-Trichloroethyl dichlorophosphate is a chemical compound that serves as an intermediate in the synthesis of various organophosphorus compounds. It is characterized by its toxic nature and potential to cause harm to both humans and the environment. Due to its hazardous properties, it can cause irritation to the skin, eyes, and respiratory tract, and may lead to more severe health effects such as nausea, vomiting, and neurological symptoms.

18868-46-7

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18868-46-7 Usage

Uses

Used in Chemical Synthesis Industry:
2,2,2-Trichloroethyl dichlorophosphate is used as a chemical intermediate for the production of organophosphorus compounds, which are essential in the manufacturing of pesticides and flame retardants. Its role in these processes is crucial for the development of effective and safe products in these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 18868-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,6 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18868-46:
(7*1)+(6*8)+(5*8)+(4*6)+(3*8)+(2*4)+(1*6)=157
157 % 10 = 7
So 18868-46-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H9N3O2/c14-13(15)10-3-1-9(2-4-10)7-12-6-5-11-8-12/h1-6,8H,7H2

18868-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trichloro-2-dichlorophosphoryloxyethane

1.2 Other means of identification

Product number -
Other names (2,2,2-Trichlorethyl)-phosphorodichloridat

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:18868-46-7 SDS

18868-46-7Upstream product

18868-46-7Relevant academic research and scientific papers

Evaluation of Natural and Synthetic Phosphate Donors for the Improved Enzymatic Synthesis of Phosphate Monoesters

Tasnádi, Gábor,Jud, Wolfgang,Hall, Mélanie,Baldenius, Kai,Ditrich, Klaus,Faber, Kurt

supporting information, p. 2394 - 2401 (2018/05/14)

Undesired product hydrolysis along with large amounts of waste in form of inorganic monophosphate by-product are the main obstacles associated with the use of pyrophosphate in the phosphatase-catalyzed synthesis of phosphate monoesters on large scale. In order to overcome both limitations, we screened a broad range of natural and synthetic organic phosphate donors with several enzymes on a broad variety of hydroxyl-compounds. Among them, acetyl phosphate delivered stable product levels and high phospho-transfer efficiency at the lower functional pH-limit, which translated into excellent productivity. The protocol is generally applicable to acid phosphatases and compatible with a range of diverse substrates. Preparative-scale transformations using acetyl phosphate synthesized from cheap starting materials yielded multiple grams of various sugar phosphates with up to 433 g L?1 h?1 space-time yield and 75% reduction of barium phosphate waste. (Figure presented.).

A NEW CONVENIENT METHOD FOR β-LACTAM FORMATION FROM β-AMINO ACIDS USING BIS(5'-NITRO-2'-PYRIDYL) 2,2,2-TRICHLOROETHYL PHOSPHATE

Kim, Sunggak,Chang, Suk Bok,Lee, Phil Ho

, p. 2735 - 2736 (2007/10/02)

Bis(5'-nitro-2'-pyridyl) 2,2,2-trichloroethyl phosphate is found to be a new efficient condensing agent for β-lactam formation from β-amino acids in acetonitrile.

O-Trihaloethyl phosphorodithioate pesticides

-

, (2008/06/13)

Compounds of the formula STR1 in which X is halogen and R1 and R2 are each alkyl groups, insecticidal, acaricidal and nematicidal compositions thereof, and a method for controlling such pests are disclosed.

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