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N-tert-Butyl-2-thiophenesulfonamide is a sulfonamide derivative featuring a tert-butyl group attached to the nitrogen atom and a thiophene ring. It is a chemical compound widely recognized for its role as a pharmaceutical intermediate and in the synthesis of various pharmaceutical drugs. N-tert-Butyl-2-thiophenesulfonamide has been studied for its potential therapeutic applications, including its use as an anticonvulsant and antihypertensive agent, and has shown promise in the development of new drugs for treating a range of medical conditions. Additionally, it has been investigated for its potential as a corrosion inhibitor in industrial applications, making it a versatile compound with applications in both pharmaceutical and industrial settings.

100342-30-1

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100342-30-1 Usage

Uses

Used in Pharmaceutical Industry:
N-tert-Butyl-2-thiophenesulfonamide is used as a pharmaceutical intermediate for the synthesis of various pharmaceutical drugs. Its unique chemical structure allows it to be a key component in the development of new medications.
Used in Therapeutic Applications:
N-tert-Butyl-2-thiophenesulfonamide is used as an anticonvulsant and antihypertensive agent, leveraging its potential therapeutic properties to manage and treat these conditions.
Used in Drug Development:
N-tert-Butyl-2-thiophenesulfonamide is utilized in the research and development of new drugs for the treatment of various medical conditions, contributing to the advancement of pharmaceutical treatments.
Used in Industrial Applications:
N-tert-Butyl-2-thiophenesulfonamide is used as a corrosion inhibitor, demonstrating its potential to protect materials from degradation in industrial settings, thereby extending their lifespan and improving efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 100342-30-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,4 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100342-30:
(8*1)+(7*0)+(6*0)+(5*3)+(4*4)+(3*2)+(2*3)+(1*0)=51
51 % 10 = 1
So 100342-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2S2/c1-8(2,3)9-13(10,11)7-5-4-6-12-7/h4-6,9H,1-3H3

100342-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-Butyl-2-thiophenesulfonamide

1.2 Other means of identification

Product number -
Other names 2-(tert-Butylaminosulfonyl)thiophene

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:100342-30-1 SDS

100342-30-1Relevant articles and documents

Zn- And Cu-catalyzed coupling of tertiary alkyl bromides and oxalates to forge challenging C?O, C?S, and C?N bonds

Gong, Yuxin,Zhu, Zhaodong,Qian, Qun,Tong, Weiqi,Gong, Hegui

supporting information, p. 1005 - 1010 (2021/02/01)

We describe here the facile construction of sterically hindered tertiary alkyl ethers and thioethers via the Zn(OTf)2catalyzed coupling of alcohols/phenols with unactivated tertiary alkyl bromides and the Cu(OTf)2-catalyzed thiolation of unactivated tertiary alkyl oxalates with thiols. The present protocol represents one of the most effective unactivated tertiary C(sp3)? heteroatom bond-forming conditions via readily accessible Lewis acid catalysis that is surprisingly less developed.

Single Peptide Backbone Surrogate Mutations to Regulate Angiotensin GPCR Subtype Selectivity

Vrettos, Eirinaios I.,Valverde, Ibai E.,Mascarin, Alba,Pallier, Patrick N.,Cerofolini, Linda,Fragai, Marco,Parigi, Giacomo,Hirmiz, Baydaa,Bekas, Nick,Grob, Nathalie M.,Stylos, Evgenios Κ.,Shaye, Hamidreza,Del Borgo, Mark,Aguilar, Marie-Isabel,Magnani, Francesca,Syed, Nelofer,Crook, Timothy,Waqif, Emal,Ghazaly, Essam,Cherezov, Vadim,Widdop, Robert E.,Luchinat, Claudio,Michael-Titus, Adina T.,Mindt, Thomas L.,Tzakos, Andreas G.

supporting information, p. 10690 - 10694 (2020/07/25)

Mutating the side-chains of amino acids in a peptide ligand, with unnatural amino acids, aiming to mitigate its short half-life is an established approach. However, it is hypothesized that mutating specific backbone peptide bonds with bioisosters can be exploited not only to enhance the proteolytic stability of parent peptides, but also to tune its receptor subtype selectivity. Towards this end, four [Y]6-Angiotensin II analogues are synthesized where amide bonds have been replaced by 1,4-disubstituted 1,2,3-triazole isosteres in four different backbone locations. All the analogues possessed enhanced stability in human plasma in comparison with the parent peptide, whereas only two of them achieved enhanced AT2R/AT1R subtype selectivity. This diversification has been studied through 2D NMR spectroscopy and unveiled a putative more structured microenvironment for the two selective ligands accompanied with increased number of NOE cross-peaks. The most potent analogue, compound 2, has been explored regarding its neurotrophic potential and resulted in an enhanced neurite growth with respect to the established agent C21.

NEW TRICYCLIC ANGIOTENSIN II AGONISTS

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Page/Page column 32, (2008/06/13)

There is provided compounds of formula (I) wherein the dotted line, X1, X2, X3, A, Y1, Y2, Y3, Y4, Z1, Z2, R2 and R3 have meanings giv

NEW BICYCLIC ANGIOTENSIN II AGONISTS

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Page/Page column 36, (2008/06/13)

There is provided a compound of formula (I) wherein R1a, R1b, X, Y1, Y2, Y3, Y4, Z1, Z2, R2 and R3 have meanings given in the description, and ph

NEW TRICYCLIC ANGIOTENSIN II AGONISTS

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Page/Page column 35, (2008/06/13)

There is provided compounds of Formula (I), wherein A, X1, X2, X3, X4, Y1, Y2, Y3, Y4, Z1, Z2, R4 and R5 have meanings given in the description, and pharmaceuticalfy-acceptable salts thereof, which compounds are useful as selective agonists of the AT2 receptor, and thus, in particular, in the treatment of inter alia gastrointestinal conditions, such as dyspepsia, IBS and MOF, and cardiovascular disorders.

NEW BICYCLIC ANGIOTENSIN II AGONISTS

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Page 36, (2010/02/07)

There is provided compounds of formula (I), wherein R1a, R1b, n, Y1, Y2, Y3, Y4, Z1, Z2, R2 and R3 have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful as selective agonists of the AT2 receptor, and thus, in particular, in the treatment of inter alia gastrointestinal conditions, such as dyspepsia, IBS and MOF, and cardiovascular disorders.

NEW TRICYCLIC ANGIOTENSIN II AGONISTS

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Page 35, (2010/02/07)

There is provided compounds of formula (I), wherein the dotted line, X1, X2, X3, A, Y1, Y2, Y3, Y4, Z1, Z2, R2 and R3 have meanings gi

NEW TRICYCLIC ANGIOTENSIN II AGONISTS

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Page 41, (2010/02/07)

There is provided compounds of formula (I), wherein the dotted lines, XI, X2, X3, X4, A, YI, Y2, Y3, Y4, ZI, Z2, R2 and R3

BICYCLIC COMPOUNDS USEFUL AS ANGIOTENSIN II AGONISTS

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Page 40, (2010/02/08)

There is provided compounds of formula I, wherein R1a, R1b, X, Y1, Y2, Y3, Y4, Z 1, Z2, R2 and R3 have meanings given in the description, and pha

Sulfonamides useful as carbonic anhydrase inhibitors

-

, (2008/06/13)

Sulfonamides and pharmaceutical compositions containing the compounds useful in controlling intraocular pressure are disclosed. Methods for controlling intraocular pressure through administration of the compositions are also disclosed.

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