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4-(1,2,3-Thiadiazol-4-yl)benzenesulfonyl chloride is an organosulfur chemical compound characterized by the presence of sulfur, chlorine, and nitrogen in its molecular structure. It is defined by a specific molecular formula and exhibits distinct melting and boiling points. 4-(1,2,3-Thiadiazol-4-yl)benzenesulfonyl chloride is predominantly used in laboratory settings and in the synthesis of other chemicals or products, where its reactivity, stability, and health and safety aspects must be carefully considered by scientists and manufacturing professionals.

499771-00-5

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499771-00-5 Usage

Uses

Used in Chemical Synthesis:
4-(1,2,3-Thiadiazol-4-yl)benzenesulfonyl chloride is used as a reagent in chemical synthesis for the preparation of various organic compounds. Its unique structure and reactivity make it a valuable component in the creation of new molecules with potential applications in pharmaceuticals, materials science, and other fields.
Used in Laboratory Research:
In the field of laboratory research, 4-(1,2,3-Thiadiazol-4-yl)benzenesulfonyl chloride serves as a key intermediate in the study of organosulfur chemistry. It is utilized to explore the properties and reactions of sulfur-containing compounds, contributing to a deeper understanding of their behavior and potential uses.
Used in Pharmaceutical Industry:
4-(1,2,3-Thiadiazol-4-yl)benzenesulfonyl chloride is used as a building block in the pharmaceutical industry for the development of new drugs. Its incorporation into drug molecules can enhance their therapeutic properties, such as improving their efficacy, selectivity, or stability.
Used in Material Science:
In material science, 4-(1,2,3-Thiadiazol-4-yl)benzenesulfonyl chloride is employed as a component in the synthesis of advanced materials with specific properties. These materials may have applications in various industries, such as electronics, coatings, or adhesives, where their unique characteristics can provide performance advantages.
Overall, 4-(1,2,3-Thiadiazol-4-yl)benzenesulfonyl chloride is a versatile organosulfur compound with a range of applications across different industries, primarily driven by its unique chemical properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 499771-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,9,7,7 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 499771-00:
(8*4)+(7*9)+(6*9)+(5*7)+(4*7)+(3*1)+(2*0)+(1*0)=215
215 % 10 = 5
So 499771-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClN2O2S2/c9-15(12,13)7-3-1-6(2-4-7)8-5-14-11-10-8/h1-5H

499771-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(thiadiazol-4-yl)benzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 4-[1,2,3]thiadiazol-4-yl-benzenesulfonyl chloride

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:499771-00-5 SDS

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