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17321-48-1

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17321-48-1 Usage

General Description

O,O-diethyl thiophosphoramidate is a chemical compound that is a type of organophosphate pesticide. It is commonly used as an insecticide and acaricide, and has been found to have moderate acute toxicity to humans and animals. O,O-diethyl thiophosphoramidate works by inhibiting the activity of acetylcholinesterase, an enzyme that is important for the proper functioning of the nervous system. Exposure to this compound can result in symptoms such as nausea, vomiting, abdominal pain, diarrhea, and muscle weakness. Long-term exposure to O,O-diethyl thiophosphoramidate has been associated with neurological disorders and chronic health effects. It is considered to be a hazardous substance and should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 17321-48-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,2 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17321-48:
(7*1)+(6*7)+(5*3)+(4*2)+(3*1)+(2*4)+(1*8)=91
91 % 10 = 1
So 17321-48-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H12NO2PS/c1-3-6-8(5,9)7-4-2/h3-4H2,1-2H3,(H2,5,9)

17321-48-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [amino(ethoxy)phosphinothioyl]oxyethane

1.2 Other means of identification

Product number -
Other names Diethyl thiophosphoramidate

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:17321-48-1 SDS

17321-48-1Relevant articles and documents

REACTION OF PHOSPHORUS THIOACID CHLORIDES WITH ETHYL ISOBUTYRIMIDATE HYDROCHLORIDE, PROPERTIES OF PHOSPHORYL THIOIMIDATES

Krongauz, Yu. I.,Potapova, V. V.,Sandakov, V. B.,Koroleva, T. N.,Bogomolova, L. M.

, p. 345 - 348 (2007/10/02)

Phosphorus thioacid chlorides react with ethyl isobutyrimidate with the formation of 1-ethoxy-1-methylpropylideneamidothiophosphates, which can be hydrolyzed at both C=N and P-N bonds.

1,3,2-Oxazaphospholidine-2-thiones from (+)-Norephedrine: Stereospecific Ring Opening, Possibly by an Elimination-Addition Mechanism

Hall, C.Richard,Inch, Thomas D.,Williams, Nancy E.

, p. 639 - 644 (2007/10/02)

1,3,2-Oxazaphospholidine-2-thiones derived from (+)-norephedrine react with alkoxide to give a product of kinetic control, formed by endocyclic P-O cleavage with inversion of configuration, and one of thermodynamic control, formed by endocyclic P-N cleavage also with inversion of configuration.It is suggested that the product of kinetic control is formed by an elimination-addition process involving a metaphosphorimidate intermediate, and that of thermodynamic control by a mechanism involving nucleophilic attack opposite endocyclic nitrogen.

Reactions of N'-cyano-N-phenylformamidine and carbodiimide with phosphorodithioic acid O,O-diethyl ester

Fedgenhaeuer,Moll

, p. 141 - 142 (2007/10/02)

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