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10252-66-1

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10252-66-1 Usage

General Description

4-[(Isopropylamino)sulfonyl]benzoic acid is a chemical compound with the formula C12H17NO4S. It is a white to off-white crystalline powder and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. The compound is also known for its anti-inflammatory and analgesic properties, and it is often used in pain relief medications. Its structure consists of a benzoic acid core with a sulfonyl group attached to an isopropylamino group. 4-[(Isopropylamino)sulfonyl]benzoic acid is compatible with other organic and inorganic chemicals and solvents, making it a versatile compound in the field of medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 10252-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10252-66:
(7*1)+(6*0)+(5*2)+(4*5)+(3*2)+(2*6)+(1*6)=61
61 % 10 = 1
So 10252-66-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO4S/c1-7(2)11-16(14,15)9-5-3-8(4-6-9)10(12)13/h3-7,11H,1-2H3,(H,12,13)/p-1

10252-66-1SDS

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 p-Isopropylsulfamoylbenzoic acid

1.2 Other means of identification

Product number -
Other names -

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:10252-66-1 SDS

10252-66-1Downstream Products

10252-66-1Relevant articles and documents

Functionalization of α-C(sp3)?H Bonds in Amides Using Radical Translocating Arylating Groups

Radhoff, Niklas,Studer, Armido

supporting information, p. 3561 - 3565 (2021/01/04)

α-C?H arylation of N-alkylamides using 2-iodoarylsulfonyl radical translocating arylating (RTA) groups is reported. The method allows the construction of α-quaternary carbon centers in amides. Various mono- and disubstituted RTA-groups are applied to the arylation of primary, secondary, and tertiary α-C(sp3)?H-bonds. These radical transformations proceed in good to excellent yields and the cascades comprise a 1,6-hydrogen atom transfer, followed by a 1,4-aryl migration with subsequent SO2 extrusion.

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