Home Sulfonamines 1129-26-6
1129-26-6,MFCD00025392
Catalog No.:AA003LKE

1129-26-6 | 4-Methoxybenzenesulfonamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$26.00   $18.00
- +
25g
95%
in stock  
$72.00   $51.00
- +
100g
95
in stock  
$253.00   $177.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003LKE
Chemical Name:
4-Methoxybenzenesulfonamide
CAS Number:
1129-26-6
Molecular Formula:
C7H9NO3S
Molecular Weight:
187.2163
MDL Number:
MFCD00025392
SMILES:
COc1ccc(cc1)S(=O)(=O)N
NSC Number:
73188
Properties
Properties
 
BP:
352.2°C at 760 mmHg  
Form:
Solid  
MP:
111-115 °C  
Refractive Index:
1.6370 (estimate)  
Storage:
Room Temperature;Keep in dry area;  

Computed Properties
 
Complexity:
224  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
0.5  

Downstream Synthesis Route

[1]Pallesen,JakobS.;Narayanan,Dilip;Tran,KimT.;Solbak,SaraM.Ø.;Marseglia,Giuseppe;Sørensen,LouisM.E.;Høj,LarsJ.;Munafò,Federico;Carmona,RosaM.C.;Garcia,AnthonyD.;Desu,HarithaL.;Brambilla,Roberta;Johansen,TommyN.;Popowicz,GrzegorzM.;Sattler,Michael;Gajhede,Michael;Bach,Anders[JournalofMedicinalChemistry,2021,vol.64,#8,p.4623-4661]

[2]Ludwig,Miroslav;Stverka,Pavel[CollectionofCzechoslovakChemicalCommunications,1996,vol.61,#8,p.1205-1214]

[3]Guenther,E.etal.[ZeitschriftfurChemie,1968,vol.8,p.111-112]

[4]Ludwig,Miroslav;Pytela,Oldrich;Kalfus,Karel;Vecera,Miroslav[CollectionofCzechoslovakChemicalCommunications,1984,vol.49,#5,p.1182-1192]

[5]Dannan;Hussain;Crooks;Dittert[JournalofPharmaceuticalSciences,1992,vol.81,#7,p.657-660]

[6]Lehr,Philipp;Billich,Andreas;Wolff,Barbara;Nussbaumer,Peter[BioorganicandMedicinalChemistryLetters,2005,vol.15,#4,p.1235-1238]

[7]Dang,Hai-Shan;Roberts,BrianP.[JournaloftheChemicalSociety.PerkintransactionsI,1996,#13,p.1493-1498]

[8]Dang,Hai-Shan;Roberts,BrianP.[JournaloftheChemicalSociety.PerkintransactionsI,1996,#13,p.1493-1498]

[9]Dang,Hai-Shan;Roberts,BrianP.[JournaloftheChemicalSociety.PerkintransactionsI,1996,#13,p.1493-1498]

[10]CurrentPatentAssignee:BOSTONSCIENTIFICCORP-US5089499,1992,A

[11]CurrentPatentAssignee:Lubrizol(in:BerkshireHathaway);BERKSHIREHATHAWAYINC-US4874894,1989,A

[12]Locationinpatent:experimentalpartVeisi,Hojat;Ghorbani-Vaghei,Ramin;Hemmati,Saba;Mahmoodi,Jafar[Synlett,2011,#16,p.2315-2320]

[13]Locationinpatent:experimentalpartVeisi,Hojat[BulletinoftheKoreanChemicalSociety,2012,vol.33,#2,p.383-386]

[14]Mita,Tsuyoshi;Higuchi,Yuki;Sato,Yoshihiro[Chemistry-AEuropeanJournal,2013,vol.19,#3,p.1123-1128]

[15]Maleki,Behrooz;Hemmati,Saba;Tayebee,Reza;Salemi,Sirous;Farokhzad,Yasaman;Baghayeri,Mehdi;Zonoz,FarrokhzadMohammadi;Akbarzadeh,Elahe;Moradi,Rohollah;Entezari,Azam;Abdi,MohammadReza;Ashrafi,SamanehSedigh;Taimazi,Fereshteh;Hashemi,Majid[HelveticaChimicaActa,2013,vol.96,#11,p.2147-2151]

[16]Zheng,Yang;Liu,Bin;Gou,Zhaopin;Li,Yao;Zhang,Xiao;Wang,Yanqing;Yu,Shujing;Li,Yonghong;Sun,Dequn[BioorganicandMedicinalChemistryLetters,2015,vol.25,#4,p.791-794]

[17]Kim,Jinho;Stahl,ShannonS.[JournalofOrganicChemistry,2015,vol.80,#4,p.2448-2454]

[18]Yang,Kai;Ke,Miaolin;Lin,Yuanguang;Song,Qiuling[GreenChemistry,2015,vol.17,#3,p.1395-1399]

[19]Zhou,Liandi;Li,Xiaokang;Liu,Wei;Zhao,Yongli;Chen,Junmin[SyntheticCommunications,2016,vol.46,#15,p.1299-1306]

[20]Wang,Bin;Tang,Lin;Liu,Liyan;Li,Yanan;Yang,Yu;Wang,Zhiyong[GreenChemistry,2017,vol.19,#24,p.5794-5799]

[21]Zhu,Kongkai;Shao,Jingwei;Tao,Hongrui;Yan,Xue;Luo,Cheng;Zhang,Hua;Duan,Wenhu[JournalofComputer-AidedMolecularDesign,2019,vol.33,#8,p.775-785]

[22]Ojha,Subhadra;Panda,Niranjan[AdvancedSynthesisandCatalysis,2020,vol.362,#3,p.561-571]

[23]Gaviria,MarioA.;Groso,EmiliaJ.;Richardson,AlistairD.;Rykaczewski,KatieA.;Schindler,CorinnaS.;Vonesh,HannahL.;Zehnder,TroyE.[OrganicLetters,2020]

[24]Chardin;Durand;Jarsalé;Rouden;Livi;Baudoux[NewJournalofChemistry,2021,vol.45,#6,p.2953-2957]

[25]Andrews,CharlotteL.;Cardozo,JoaquinM.;Chow,AlyssaS.;Crainic,JenniferA.;Parsons,WilliamH.;Rutland,NicholasT.;Sheehan,BrendanK.[BioorganicandMedicinalChemistryLetters,2021,vol.49]

[26]Govindan,Karthick;Chen,Nian-Qi;Chuang,Yu-Wei;Lin,Wei-Yu[OrganicLetters,2021,vol.23,#24,p.9419-9424]

19829-29-9    29917-03-1    2645-22-9    1129-26-6   
Natrium-N,N'-bis(p-methoxyphenylsulfonyl)-S-(4-pyridyl)sulfodiimidat 

[1]Phosphorus,SulfurandSiliconandtheRelatedElements,1990,vol.53,p.313-326

[1]Aizina,Yu.A.;Rozentsveig;Popov;Levkovskaya[RussianJournalofOrganicChemistry,2017,vol.53,#11,p.1753-1755][Zh.Org.Khim.,2017,vol.53,#11,p.1714-1716,3]

[2]Boberg,Friedrich;Paetz,Andrea;Bruchmann,Bernd;Garming,Alfons[PhosphorusandSulfurandtheRelatedElements,1987,vol.33,p.99-108]

1129-26-6    98-68-0   
4-methoxy-N-(4-methoxyphenyl)sulfonylbenzenesulfonamide 

[1]Jeong,Yuri;Ban,Jaeyoung;Lim,Minkyung;Rhee,Hakjune[Synthesis,2018,vol.50,#9,p.1867-1874]

[2]Ludwig,Miroslav;Stverka,Pavel[CollectionofCzechoslovakChemicalCommunications,1996,vol.61,#8,p.1205-1214]

[3]Chardin;Durand;Jarsalé;Rouden;Livi;Baudoux[NewJournalofChemistry,2021,vol.45,#6,p.2953-2957]

[4]Pei,Mengxue;Zu,Conghui;Liu,Zhen;Yang,Fan;Wu,Yangjie[JournalofOrganicChemistry,2021,vol.86,#17,p.11324-11332]

[1]CurrentPatentAssignee:HARVARDUNIVERSITY-WO2012/24604,2012,A2Locationinpatent:Page/Pagecolumn77-78

[2]Taylor,Sophia;Gullick,John;McMorn,Paul;Bethell,Donald;Page,PhilipC.Bulman;Hancock,FrederickE.;King,Frank;Hutchings,GrahamJ.[JournaloftheChemicalSociety.PerkinTransactions2(2001),2001,#9,p.1714-1723]

[3]Müller,Paul;Baud,Corine;Jacquier,Yvan[CanadianJournalofChemistry,1998,vol.76,#6,p.738-750]

Literature

Title: Correlation analyses on binding affinity of substituted benzenesulfonamides with carbonic anhydrase using ab initio MO calculations on their complex structures (II).

Journal: Bioorganic & medicinal chemistry letters 20110101

Title: Entropic contribution to the linking coefficient in fragment based drug design: a case study.

Journal: Journal of medicinal chemistry 20100527

Title: Novel use of chemical shift in NMR as molecular descriptor: a first report on modeling carbonic anhydrase inhibitory activity and related parameters.

Journal: Bioorganic & medicinal chemistry letters 20050215

Title: Topological modeling of lipophilicity, diuretic activity, and carbonic inhibition activity of benzene sulfonamides: a molecular connectivity approach.

Journal: Bioorganic & medicinal chemistry letters 20041115

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:1129-26-6 Molecular Formula|1129-26-6 MDL|1129-26-6 SMILES|1129-26-6 4-Methoxybenzenesulfonamide