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Benzenesulfonyl semicarbazide is a chemical compound with the chemical formula C7H9N3O3S, having an average mass of 213.23240 Da. It is typically white to ivory in color and appears as a crystalline solid. Benzenesulfonyl semicarbazide is highly stable under regular conditions, but it can cause respiratory tract irritation when ingested, inhaled, or comes into contact with the skin, necessitating safety precautions during handling. It is particularly valuable in medical and chemical research due to its role in synthesizing other organic compounds or medicines, as it facilitates chemical reactions.

10195-68-3

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10195-68-3 Usage

Uses

Used in Scientific Experiments:
Benzenesulfonyl semicarbazide is used as a reagent in various scientific experiments for its ability to participate in chemical reactions, making it a valuable component in research settings.
Used in Industrial Processes:
In industrial applications, Benzenesulfonyl semicarbazide is used as an intermediate in the synthesis of other organic compounds, contributing to the production of various chemical products.
Used in Pharmaceutical Synthesis:
Benzenesulfonyl semicarbazide is used as a key component in the synthesis of certain medicines, leveraging its reactivity to facilitate the creation of pharmaceutical compounds. This makes it an essential part of the drug development process in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 10195-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,9 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10195-68:
(7*1)+(6*0)+(5*1)+(4*9)+(3*5)+(2*6)+(1*8)=83
83 % 10 = 3
So 10195-68-3 is a valid CAS Registry Number.

10195-68-3SDS

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 benzenesulfonamidourea

1.2 Other means of identification

Product number -
Other names Phenylsulfonyl-semicarbazid

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:10195-68-3 SDS

10195-68-3Relevant academic research and scientific papers

An efficient synthesis of sulfonylhydrazides and sulfonylsemicarbazides by utilizing alumina as a catalyst

Safaei-Ghomi, Javad

, p. 1561 - 1563 (2008/09/16)

Sulfonyl hydrazides and sulfonyl semicarbazides are readily prepared by the reacting of hydrazine derivatives with sulfonyl chlorides in the presence of basic alumina under solvent-free conditions. Reaction of a sulfonyl chloride with t-butylcarbazate, followed by hydrolysis provides the corresponding sulfonyl hydrazides in higher yield and shorter time than previously reported.

A convenient procedure for the preparation of sulfonamidoureas using triphosgene

Safaei-Ghomi, Javad,Bamoniri, Abdolhamid,Abbaszadeh-Nooshabady, Aboalfazl

, p. 721 - 724 (2008/10/09)

An efficient method for the preparation of sulfonamidourea using triphosgene in organic solvents is reported. Sulfonylhydrazides and acetylsulfanilylhydrazide were transformed into the corresponding intermediates using triphosgene in 1,4-dioxane/water or tetrahydrofuran as solvents. These intermediates were converted in situ into symmetrical and unsymmetrical sulfonamidoureas in high yields and shorter periods of time related to previous methods.

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