产品编号 A110561 | CAS号 7773-06-0 | Aladdin
Ammonium sulfamate
货号 规格 库存 价格 数量
A110561-100g AR,99.0% 上海(预计4-8周)
A110561-25g AR,99.0% 上海(>10)


密度 1.8000
熔点 131-135°C
存贮条件 密封干燥保存。


产品介绍 Ammonium sulfamate is a weak oxidizing agent. Commonly used as a broad spectrum herbicide, with additional uses as a compost accelerator and in industrial processes.
别名 磺酸铵;Aminosulfonic Acid Ammonium Salt; Ammonium Amidosulfate; Sulfamic Acid Ammonium Salt Sulfamic Acid Ammonium Salt
应用 A weakly oxidizing agent employed as a broad-spectrum herbicide.
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标识符号 GHS07 GHS07, GHS09 GHS09
信号词 Warning
风险声明 (欧洲) R22
安全声明(欧洲) S24/25
警示性声明 P273
危害码(欧洲) Xn
危害声明 H302,H400
个人防护设备 dust mask type N95 (US),Eyeshields,Gloves
RTECS WO6125000
WGK德国 3
Merck Index 554
UN代码 3077
M K Marchewka, M Drozd
Crystalline complexes between ethylenediammonium dication and terephthalate, chloroacetate, phosphite, selenite and sulfamate anions were obtained by slow evaporation from water solution method. Room ...Read More
Toolika Agrawal, Silas P Cook
The iron-catalyzed cross-coupling of aryl sulfamates and tosylates has been achieved with primary and secondary alkyl Grignards. This study of iron-catalyzed cross-coupling reactions also examines the...Read More
Jean-Yves Winum, Pedro A Colinas, Claudiu T Supuran
Targeting tumour associated carbonic anhydrase (CA, EC isoforms IX and XII is now considered as a pertinent approach for the development of new cancer therapeutics against hypoxic tumours. In...Read More
Tristan T Reuillon, Annalisa A Bertoli, Roger J RJ Griffin, Duncan C DC Miller, Bernard T BT Golding
Sulfamates are important functional groups in certain areas of current medicinal chemistry and drug development. Alcohols and phenols are generally converted into the corresponding primary sulfamates ...Read More
Philip T Cherian, Jiangwei Yao, Roberta Leonardi, Marcus M Maddox, Vicki A Luna, Charles O Rock, Richard E Lee
PlsY is the essential first step in membrane phospholipid synthesis of Gram-positive pathogens. PlsY catalyzes the transfer of the fatty acid from acyl-phosphate to the 1-position of glycerol-3-phosph...Read More
Jean-Yves Winum, Fabrizio Carta, Carol Ward, Peter Mullen, David Harrison, Simon P Langdon, Alessandro Cecchi, Andrea Scozzafava, Ian Kunkler, Claudiu T Supuran
A series of 50 sulfamates were obtained by reacting 4-aminophenol with isocyanates followed by sulfamoylation. Most of the new compounds were nanomolar inhibitors of the tumor-associated carbonic anhy...Read More
Na N Zhang, David J DJ Hoffman, Nicholas N Gutsche, Jayesh J Gupta, Virgil V Percec
The efficiency of arylboron-based nucleophiles, boronic acid, potassium trifluoroborate, neopentylglycolboronate, and pinacol boronate in nickel-catalyzed Suzuki-Miyaura cross-coupling reactions with ...Read More
Christopher S CS Adams, Luke A LA Boralsky, Ilia A IA Guzei, Jennifer M JM Schomaker
Nitrogen-containing stereotriads, compounds with three adjacent stereodefined carbons, are commonly found in biologically important molecules. However, the preparation of molecules bearing these motif...Read More
Danielle C Lohman, Richard Wolfenden, David R Edwards
The final step in the degradation of heparin sulfate involves the enzymatic hydrolysis of its 2-sulfamido groups. To evaluate the power of the corresponding sulfamidases as catalysts, we examined the ...Read More
Anna A Ohradanova, Daniela D Vullo, Silvia S Pastorekova, Jaromir J Pastorek, Daniel J DJ Jackson, Gert G W?rheide, Claudiu T CT Supuran
The α-carbonic anhydrase (CA, EC Astrosclerin-3 previously isolated from the living fossil sponge Astrosclera willeyana (Jackson et al., Science 2007, 316, 1893), was cloned, kinetically cha...Read More
Jesse J Chen, Christopher A Tsu, James M Gavin, Michael A Milhollen, Frank J Bruzzese, William D Mallender, Michael D Sintchak, Nancy J Bump, Xiaofeng Yang, Jingya Ma, Huay-Keng Loke, Qing Xu, Ping Li, Neil F Bence, James E Brownell, Lawrence R Dick
Ubiquitin-activating enzyme (UAE or E1) activates ubiquitin via an adenylate intermediate and catalyzes its transfer to a ubiquitin-conjugating enzyme (E2). MLN4924 is an adenosine sulfamate analogue ...Read More
Dengfeng Dou, Kok-Chuan Tiew, Guijia He, Sivakoteswara Rao Mandadapu, Sridhar Aravapalli, Kevin R Alliston, Yunjeong Kim, Kyeong-Ok Chang, William C Groutas
A new class of compounds that exhibit anti-norovirus activity in a cell-based system and embody in their structure a cyclosulfamide scaffold has been identified. The structure of the initial hit (comp...Read More
Derek J DJ Langeslay, Szabolcs S Beni, Cynthia K CK Larive
Sulfamate (NHSO(3)(-)) groups are critically important structural elements of the glycosaminoglycans heparin and heparan sulfate (HS). Experimental conditions are presented for detection of the sulfam...Read More
Laszlo Tarko, Claudiu T Supuran
The last version of the PRECLAV algorithm was used to investigate a series of sulfamate/sulfamide carbonic anhydrase (CA, EC inhibitors. PRECLAV allows identification of outliers for lead hop...Read More
Ning Dai, Amisha D Shah, Lanhua Hu, Michael J Plewa, Bruce McKague, William A Mitch
With years of full-scale experience for precombustion CO(2) capture, amine-based technologies are emerging as the prime contender for postcombustion CO(2) capture. However, concerns for postcombustion...Read More
Amit A Saha, R B Nasir RB Baig, John J Leazer, Rajender S RS Varma
Unnatural α-amino acids containing dithiocarbamate side chains were synthesized by a one-pot reaction of in situ generated dithiocarbamate anions with sulfamidates. A wide range of these anions parti...Read More
Derek J DJ Langeslay, Robert P RP Young, Szabolcs S Beni, Consuelo N CN Beecher, Leonard J LJ Mueller, Cynthia K CK Larive
Sulfamate groups (NHSO(3)(-)) are important structural elements in the glycosaminoglycans (GAGs) heparin and heparan sulfate (HS). In this work, proton nuclear magnetic resonance (NMR) line-shape anal...Read More
Edward J EJ Emmett, Charlotte S CS Richards-Taylor, Bao B Nguyen, Alfonso A Garcia-Rubia, Barry R BR Hayter, Michael C MC Willis
By using DABCO·(SO(2))(2), DABSO, as a solid bench-stable SO(2)-equivalent, the palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides has been achieved. N,N-Dialkylhydrazin...Read More
Keisuke K Takahashi, Daisuke D Yamaguchi, Jun J Ishihara, Susumi S Hatakeyama
A total synthesis of (-)-kaitocephalin, an ionotropic glutamate receptor antagonist, is accomplished in highly stereocontrolled manner via Overman rearrangement, rhodium-catalyzed benzylic C-H aminati...Read More
Daniel Can, Bernhard Spingler, Paul Schmutz, Filipa Mendes, Paula Raposinho, Célia Fernandes, Fabrizio Carta, Alessio Innocenti, Isabel Santos, Claudiu T Supuran, Roger Alberto
Enhanced receptor selectivity: carbonic anhydrase inhibitors are relevant for both cancer diagnosis and therapy. Combining non-radioactive Re compounds with their radioactive (99m)Tc homologs enables ...Read More
Patricia P Chávez, Jonathan J Kirsch, Jan J Streuff, Kilian K Mu?iz
An intramolecular diamination of acrylates is reported using sulfamates as nitrogen sources. This reaction proceeds under palladium(II) catalysis with copper bromide as oxidant and gives rise to anti-...Read More
Marie M Lopez, Hoan H Vu, Conan K CK Wang, Maarten G MG Wolf, Gerrit G Groenhof, Alessio A Innocenti, Claudiu T CT Supuran, Sally-Ann SA Poulsen
Carbonic anhydrases (CAs) are enzymes whose endogenous reaction is the reversible hydration of CO(2) to give HCO(3)(-) and a proton. CA are also known to exhibit weak and promiscuous esterase activity...Read More