Cas no 60858-95-9 (Diazald-N-methyl-13C)
Diazald-N-methyl-13C structure
Product Name:Diazald-N-methyl-13C
CAS No:60858-95-9
MF:C8H10N2O3S
MW:215.234255313873
CID:57607
PubChem ID:10900021
Update Time:2025-04-18
Diazald-N-methyl-13C Chemical and Physical Properties
Names and Identifiers
-
- Diazald-N-methyl-13C
- N-Methyl-13C-N-nitroso-p-toluenesulfonamide
- N-METHYL-N-NITROSO-P-TOLUENESULFONAMIDE-13C
- [methyl-13C]N-methyl-N-nitroso-4-toluenesulfonic acid amide
- 13-(1-cyclopent-2-enyl)-N-[4-(pyridin-2-ylsulfamoyl)phenyl]tridecanami de
- N-[13-((R)-cyclopent-2-enyl-tridecanoyl]-sulfanilic acid-[2]pyridylamide
- N-[13-((R)-Cyclopent-2-enyl-tridecanoyl]-sulfanilsaeure-[2]pyridylamid
- N-[13C]methyl-N-nitroso-p-toluenesulfonamide
- p-Tolylsulfonyl-< 13C> -methylnitrosoamid
- Diazald(R)-N-methyl-13C-N-methyl-d3
- 60858-95-9
- Diazald(R)-(N-methyl-13C), 99 atom % 13C, 97% (CP)
- 102832-11-1
-
- Inchi： 1S/C8H10N2O3S/c1-7-3-5-8(6-4-7)14(12,13)10(2)9-11/h3-6H,1-2H3/i2+1
- InChI Key： FFKZOUIEAHOBHW-VQEHIDDOSA-N
- SMILES： S(C1C=CC(C)=CC=1)(N([13CH3])N=O)(=O)=O
Computed Properties
- Exact Mass: 215.04456819g/mol
- Monoisotopic Mass: 215.04456819g/mol
- Isotope Atom Count: 1
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 14
- Rotatable Bond Count: 2
- Complexity: 288
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 0.6
- Topological Polar Surface Area: 75.2?2
Experimental Properties
- Density: 1.3
- Melting Point: 61-62 oC
- Refractive Index: 1.572
Diazald-N-methyl-13C Security Information
- Hazardous Material transportation number：UN 2811
- WGK Germany：3
- Hazard Category Code： R20/21/22;R43
- Safety Instruction： S26;S36
-
Hazardous Material Identification：
- HazardClass：6.1(b)
- PackingGroup：III
- Risk Phrases：R20/21/22;R43
- Safety Term：S26;S36
- Packing Group：III
- Hazard Level：6.1(b)
Diazald-N-methyl-13C Related Literature
-
Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
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Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
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Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
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