20607-43-6 Usage
Uses
Used in Organic Synthesis:
Sodium 2-propanethiolate is used as a reagent in organic synthesis for the preparation of various organic compounds, such as thioethers, sulfides, and thioesters. Its properties facilitate the formation of these compounds, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, sodium 2-propanethiolate is utilized in the manufacturing process of various drugs. Its reactivity and solubility make it a valuable component in the synthesis of pharmaceuticals, aiding in the development of new medications.
Used in Pesticide Production:
Sodium 2-propanethiolate also finds application in the production of pesticides. Its role in the synthesis of these agricultural chemicals helps in creating effective pest control solutions, contributing to increased crop yields and protection against pests.
Used in Other Industrial Products:
Beyond the aforementioned industries, sodium 2-propanethiolate is employed in the manufacturing of a range of other industrial products. Its versatility in chemical reactions and solubility in water make it a useful component in various industrial applications.
It is crucial to handle sodium 2-propanethiolate with care due to its potential toxicity if ingested or inhaled, as well as its ability to cause skin and eye irritation. Proper safety measures should be taken during its use in laboratory and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 20607-43-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,0 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20607-43:
(7*2)+(6*0)+(5*6)+(4*0)+(3*7)+(2*4)+(1*3)=76
76 % 10 = 6
So 20607-43-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H8S.Na/c1-3(2)4;/h3-4H,1-2H3;/q;+1/p-1/rC3H7NaS/c1-3(2)5-4/h3H,1-2H3
20607-43-6Relevant articles and documents
Design and synthesis of new 4-alkylthio monocyclic β-lactams
Lee, Sang Hyup
, p. 121 - 127 (2013/08/24)
New types of monocyclic β-lactams constitute an important class of compounds due to their unique structures and natures. Here, the design and synthesis of new 4-alkylthio monocyclic β-lactams 2a and 3a are reported. Significantly, compounds 2a and 3a, while keeping a monocyclic system, were designed to contain all of the substructures provided by the cleavage of C(2)-C(3) bond in penicillins. Efficient synthetic pathways for compounds 2a and 3a were established based on two different strategies. Compound 2a was synthesized from raw materials, using 4-acetoxyazetidin-2-one as a key intermediate, through a ten-step synthetic sequence in 3% overall yield. Compound 3a was synthesized from potassium salt of penicillin G (17), using the degraded product 20 as a key intermediate, through a six-step synthetic sequence in 11% overall yield. 4-Alkylthioazetidin- 2-one derivatives, introduced in this study, could serve as valuable intermediates for the development of new monocyclic β-lactams.
Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity
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Page/Page column 22, (2010/02/14)
The present application describes modulators of MCP-1 of formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, wherein X, Z, a, b, c, d, n, R1, R2, R3, R4, R5, R10, R
Process for producing arylsulfenyl halide
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Page/Page column 7, (2010/11/29)
A process for producing a compound of the formula (II): wherein Hal1 represents halogen and R1 and R2 each independently represents halogen, alkyl, alkoxy, nitro or cyano, which comprises allowing a halogenating agent to react with a compound of the formula (I): wherein Alk represents branched alkyl and R1 and R2 are as defined above.
