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26118-67-2

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26118-67-2 Usage

Description

Isopropylsulphamoyl chloride is a chemical compound that serves as a key reactant in the synthesis of N-Alkylsulfamic Acid Derivatives. It is characterized by its reactive nature and ability to form various chemical bonds, making it a versatile component in organic chemistry.

Uses

Used in Chemical Synthesis:
Isopropylsulphamoyl chloride is used as a reactant for the synthesis of N-Alkylsulfamic Acid Derivatives. Its reactivity allows it to participate in various chemical reactions, contributing to the formation of a wide range of compounds with diverse applications across different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, isopropylsulphamoyl chloride is used as an intermediate in the production of various drugs and pharmaceutical compounds. Its ability to form stable bonds with other molecules makes it a valuable component in the development of new medications and therapies.
Used in Agrochemical Industry:
Isopropylsulphamoyl chloride is also utilized in the agrochemical industry for the synthesis of various agrochemical products, such as pesticides and herbicides. Its role in creating stable and effective compounds contributes to the development of more efficient and environmentally friendly solutions for agricultural applications.
Used in Research and Development:
In research and development settings, isopropylsulphamoyl chloride is employed as a key reactant in the exploration of new chemical reactions and the discovery of novel compounds. Its versatility and reactivity make it an essential tool for advancing scientific knowledge and innovation in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 26118-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,1 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26118-67:
(7*2)+(6*6)+(5*1)+(4*1)+(3*8)+(2*6)+(1*7)=102
102 % 10 = 2
So 26118-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H8ClNO2S/c1-3(2)5-8(4,6)7/h3,5H,1-2H3

26118-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Isopropylsulfamoyl chloride

1.2 Other means of identification

Product number -
Other names N-propan-2-ylsulfamoyl 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:26118-67-2 SDS

26118-67-2Relevant articles and documents

2,1,3-Benzothiadiazine derivatives: Synthesis and screening versus PDE4 enzyme

Tait, Annalisa,Luppi, Amedeo,Avallone, Rossella,Baraldi, Mario

, p. 653 - 663 (2007/10/03)

A series of N-1,3 disubstituted 2,1,3-benzothiadiazine derivatives (BTDs) were synthesized and evaluated for their inhibitory activity versus enzymatic isoform PDE4 extracted from U937 cell line. Some of the tested compounds showed a high PDE4 inhibitory activity at 100:μM and the IC50 value of the most interesting terms were evaluated. The structure-activity relationships of these compounds showed that the 3,5-di-tert-butyl-4-hydroxybenzyl moiety at N-1 position is important to obtain activity at micromolar level as previously reported. For the same compounds the antioxidant activity were evaluated highlighting 14 as the most significative one. The introduction of other bulky substituents in N-1 position is detrimental.

3-Azabicyclo[3.1.0]hexane derivatives useful in therapy

-

, (2008/06/13)

Compounds of formula (I), their salts and prodrugs thereof, where the substituents are as defined herein are disclosed as opiate binding agents useful in the treatment of opiate-mediated conditions. Also described are processes for making such substances.

Sulfamates as antiglaucoma agents

-

, (2008/06/13)

Sulfamate esters of the formula where A is aryloxyalkyl, p is the number of unreacted hydroxy groups present on the alkyl moiety and may be zero, z is the number of --OS(O)2 NR1 R2 groups attached to carbons of the alkyl moiety and is always at least one; R1 and R2 are selected from hydrogen, loweralkyl, carboxy, and the like are useful in treating glaucoma.

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