61704-46-9 Usage
Uses
Used in Organic Synthesis:
1,4-Dithiane, 2,5-bis(chloromethyl)is used as a protecting group for aldehydes and ketones, allowing chemists to perform selective functionalization in complex organic synthesis. This application is crucial for the development of new pharmaceuticals and other biologically active molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,4-Dithiane, 2,5-bis(chloromethyl)is utilized in the preparation of various drugs. Its ability to protect sensitive functional groups during synthesis contributes to the production of more effective and safer medications.
Used in Agrochemical Production:
1,4-Dithiane, 2,5-bis(chloromethyl)serves as a key intermediate in the synthesis of agrochemicals, which are essential for crop protection and enhancement of agricultural productivity.
Used in Fine Chemicals Industry:
1,4-Dithiane, 2,5-bis(chloromethyl)is also used in the production of fine chemicals, which are high-purity chemicals used in various applications, including research, pharmaceuticals, and specialty industries.
Used in Research and Development:
1,4-Dithiane, 2,5-bis(chloromethyl)is employed as a reagent in the modification of natural products and bioactive molecules, facilitating advancements in chemical research and the discovery of new chemical entities with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 61704-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,0 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61704-46:
(7*6)+(6*1)+(5*7)+(4*0)+(3*4)+(2*4)+(1*6)=109
109 % 10 = 9
So 61704-46-9 is a valid CAS Registry Number.
61704-46-9Relevant academic research and scientific papers
PREPARATION METHOD OF THIOL COMPOUND
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Paragraph 0132-0139, (2020/04/17)
Embodiments relate to a method for manufacturing a thiol compound with high purity and high yield, which does not require cryogenic reaction conditions, does not require additional special equipment, and increases the amount of production per hour. The manufacturing method comprises following steps of: obtaining a sulfur-containing heterocyclic compound from a thioepoxy-based compound obtained by conducting a reaction of an epoxy-based compound with a sulfide; and conducting a reaction of the sulfur-containing heterocyclic compound with a thiolating agent.COPYRIGHT KIPO 2020
''DOPING EFFECT'' OF LITHIUM PERCHLORATE IN THE ACID-CATALYZED OPENING OF THIIRANES AND THIETANE. FORMATION OF 1,4-DITHIANES AND MERCAPTOALKYL PERCHLORATES.
Magerramov, A. M.,Tagirova, S. V.,Allakhverdiev, M. A.,Zhdankin, V. V.,Kozmin, A. S.,Zefirov, N. S.
, p. 687 - 689 (2007/10/02)
Substituted thiiranes react with acetic acid in the presence of lithium perchlorate with the formation of cyclic dimers, i.e., the corresponding substituted 1,4-dithianes.The main product in the analogous reaction of substituted thietane is the corresponding mercaptoalkyl perchlorate.
