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28-5700

氨基磺酸

Name: 氨基磺酸
Brand: SAJ

JIS special grade, ≥99.5%

别名:

磺酰胺酸

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关于此项目

线性分子式:

NH₂SO₃H

化学文摘社编号:

5329-14-6

分子量:

97.09

UNSPSC Code:

12352106

PubChem Substance ID:

329753241

EC Number:

226-218-8

MDL number:

MFCD00011603

Assay:

≥99.5%

Form:

solid

Grade:

JIS special grade

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grade

JIS special grade

assay

≥99.5%

form

solid

availability

available only in Japan

mp

215-225 °C (dec.) (lit.)

solubility

water: 213 g/L at 20 °C, water: 470 g/L at 80 °C

density

2.151 g/cm³ at 25 °C

SMILES string

NS(O)(=O)=O

InChI

1S/H3NO3S/c1-5(2,3)4/h(H3,1,2,3,4)

InChI key

IIACRCGMVDHOTQ-UHFFFAOYSA-N

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pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H412

pcodes

P273 - P305 + P351 + P338

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Derek J Langeslay et al.

Analytical chemistry, 83(20), 8006-8010 (2011-09-15)

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 sulfamate (1)H NMR resonances in aqueous solution. NMR spectra reported for N-sulfoglucosamine (GlcNS) and the synthetic

Iron-catalyzed cross-coupling reactions of alkyl Grignards with aryl sulfamates and tosylates.

Toolika Agrawal et al.

Organic letters, 15(1), 96-99 (2012-12-19)

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 isomerization and β-hydride elimination problems that are associated with the use of isopropyl nucleophiles.

Glycosidic carbonic anhydrase IX inhibitors: a sweet approach against cancer.

Jean-Yves Winum et al.

Bioorganic & medicinal chemistry, 21(6), 1419-1426 (2012-12-04)

Targeting tumour associated carbonic anhydrase (CA, EC 4.2.1.1) isoforms IX and XII is now considered as a pertinent approach for the development of new cancer therapeutics against hypoxic tumours. In the last period, with the help of X-ray crystallography, much

[(Cp-R)M(CO)3] (M=Re or 99mTc) Arylsulfonamide, arylsulfamide, and arylsulfamate conjugates for selective targeting of human carbonic anhydrase IX.

Daniel Can et al.

Angewandte Chemie (International ed. in English), 51(14), 3354-3357 (2012-02-22)

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 the use of identical molecules for therapy and imaging (theragnostic). The syntheses and in vitro evaluation

Modular functionalization of allenes to aminated stereotriads.

Christopher S Adams et al.

Journal of the American Chemical Society, 134(26), 10807-10810 (2012-06-20)

Nitrogen-containing stereotriads, compounds with three adjacent stereodefined carbons, are commonly found in biologically important molecules. However, the preparation of molecules bearing these motifs can be challenging. Herein, we describe a modular oxidation protocol which converts a substituted allene to a

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